TECTA: Difference between revisions

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Latest revision as of 22:43, 23 December 2017

Alpha-tectorin is a protein that in humans is encoded by the TECTA gene.^[1]^[2]^[3]

The tectorial membrane is an extracellular matrix of the inner ear that contacts the stereocilia bundles of specialized sensory hair cells. Sound induces movement of these hair cells relative to the tectorial membrane, deflects the stereocilia, and leads to fluctuations in hair-cell membrane potential, transducing sound into electrical signals. Alpha-tectorin is one of the major noncollagenous components of the tectorial membrane. Mutations in the TECTA gene have been shown to be responsible for autosomal dominant nonsyndromic hearing impairment and a recessive form of sensorineural pre-lingual non-syndromic deafness.^[3]

References

↑ Hughes DC, Legan PK, Steel KP, Richardson GP (Apr 1998). "Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness". Genomics. 48 (1): 46–51. doi:10.1006/geno.1997.5159. PMID 9503015.
↑ Verhoeven K, Van Laer L, Kirschhofer K, Legan PK, Hughes DC, Schatteman I, Verstreken M, Van Hauwe P, Coucke P, Chen A, Smith RJ, Somers T, Offeciers FE, Van de Heyning P, Richardson GP, Wachtler F, Kimberling WJ, Willems PJ, Govaerts PJ, Van Camp G (May 1998). "Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment". Nat Genet. 19 (1): 60–2. doi:10.1038/ng0598-60. PMID 9590290.
↑ ^3.0 ^3.1 "Entrez Gene: TECTA tectorin alpha".

Van Camp G, Willems PJ, Smith RJ (1997). "Nonsyndromic hearing impairment: unparalleled heterogeneity". Am. J. Hum. Genet. 60 (4): 758–64. PMC 1712474. PMID 9106521.
Verhoeven K, Van Camp G, Govaerts PJ, et al. (1997). "A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24". Am. J. Hum. Genet. 60 (5): 1168–73. PMC 1712440. PMID 9150164.
Balciuniene J, Dahl N, Borg E, et al. (1998). "Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family". Am. J. Hum. Genet. 63 (3): 786–93. doi:10.1086/302012. PMC 1377400. PMID 9718342.
Mustapha M, Weil D, Chardenoux S, et al. (1999). "An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21". Hum. Mol. Genet. 8 (3): 409–12. doi:10.1093/hmg/8.3.409. PMID 9949200.
Alloisio N, Morlé L, Bozon M, et al. (1999). "Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss". Eur. J. Hum. Genet. 7 (2): 255–8. doi:10.1038/sj.ejhg.5200273. PMID 10196713.
Balciuniene J, Dahl N, Jalonen P, et al. (2000). "Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypes". Hum. Genet. 105 (3): 211–6. doi:10.1007/s004390051091. PMID 10987647.
Moreno-Pelayo MA, del Castillo I, Villamar M, et al. (2001). "A cysteine substitution in the zona pellucida domain of α-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family". J. Med. Genet. 38 (5): E13. doi:10.1136/jmg.38.5.e13. PMC 1734870. PMID 11333869.
Iwasaki S, Harada D, Usami S, et al. (2002). "Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss". Arch. Otolaryngol. Head Neck Surg. 128 (8): 913–7. doi:10.1001/archotol.128.8.913. PMID 12162770.
Naz S, Alasti F, Mowjoodi A, et al. (2003). "Distinctive audiometric profile associated with DFNB21 alleles of TECTA". J. Med. Genet. 40 (5): 360–3. doi:10.1136/jmg.40.5.360. PMC 1735454. PMID 12746400.
Pfister M, Thiele H, Van Camp G, et al. (2005). "A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations". Cell. Physiol. Biochem. 14 (4–6): 369–76. doi:10.1159/000080347. PMID 15319541.
Plantinga RF, de Brouwer AP, Huygen PL, et al. (2006). "A Novel TECTA Mutation in a Dutch DFNA8/12 Family Confirms Genotype–Phenotype Correlation". J. Assoc. Res. Otolaryngol. 7 (2): 173–81. doi:10.1007/s10162-006-0033-z. PMC 2504577. PMID 16718611.
Plantinga RF, Cremers CW, Huygen PL, et al. (2007). "Audiological Evaluation of Affected Members from a Dutch DFNA8/12 (TECTA) Family". J. Assoc. Res. Otolaryngol. 8 (1): 1–7. doi:10.1007/s10162-006-0060-9. PMC 2538417. PMID 17136632.
Meyer NC, Alasti F, Nishimura CJ, et al. (2007). "Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus". Am. J. Med. Genet. A. 143 (14): 1623–9. doi:10.1002/ajmg.a.31718. PMID 17431902.
Meyer NC, Nishimura CJ, McMordie S, Smith RJ (2007). "Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigree". Clin. Genet. 72 (2): 130–7. doi:10.1111/j.1399-0004.2007.00828.x. PMID 17661817.

This article on a gene on human chromosome 11 is a stub. You can help Wikipedia by expanding it.

[pmid9503015-1] Hughes DC, Legan PK, Steel KP, Richardson GP (Apr 1998). "Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness". Genomics. 48 (1): 46–51. doi:10.1006/geno.1997.5159. PMID 9503015.

[pmid9590290-2] Verhoeven K, Van Laer L, Kirschhofer K, Legan PK, Hughes DC, Schatteman I, Verstreken M, Van Hauwe P, Coucke P, Chen A, Smith RJ, Somers T, Offeciers FE, Van de Heyning P, Richardson GP, Wachtler F, Kimberling WJ, Willems PJ, Govaerts PJ, Van Camp G (May 1998). "Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment". Nat Genet. 19 (1): 60–2. doi:10.1038/ng0598-60. PMID 9590290.

[entrez-3] 3.0 ^3.1 "Entrez Gene: TECTA tectorin alpha".

[1]

[2]

[3]

@@ Line 1: / Line 1: @@
-<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
+{{for|Tecta, a brand of a proton pump inhibitor drug|Pantoprazole}}
-{{PBB_Controls
+{{Infobox_gene}}
-| update_page = yes
+'''Alpha-tectorin''' is a [[protein]] that in humans is encoded by the ''TECTA'' [[gene]].<ref name="pmid9503015">{{cite journal |vauthors=Hughes DC, Legan PK, Steel KP, Richardson GP | title = Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness | journal = Genomics | volume = 48 | issue = 1 | pages = 46–51 |date=Apr 1998 | pmid = 9503015 | pmc =  | doi = 10.1006/geno.1997.5159 }}</ref><ref name="pmid9590290">{{cite journal |vauthors=Verhoeven K, Van Laer L, Kirschhofer K, Legan PK, Hughes DC, Schatteman I, Verstreken M, Van Hauwe P, Coucke P, Chen A, Smith RJ, Somers T, Offeciers FE, Van de Heyning P, Richardson GP, Wachtler F, Kimberling WJ, Willems PJ, Govaerts PJ, Van Camp G | title = Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment | journal = Nat Genet | volume = 19 | issue = 1 | pages = 60–2 |date=May 1998 | pmid = 9590290 | pmc =  | doi = 10.1038/ng0598-60 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: TECTA tectorin alpha| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7007| accessdate = }}</ref>
-| require_manual_inspection = no
-| update_protein_box = yes
-| update_summary = yes
-| update_citations = yes
-}}
-<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
-{{GNF_Protein_box
- | image =
- | image_source =
- | PDB =
- | Name = Tectorin alpha
- | HGNCid = 11720
- | Symbol = TECTA
- | AltSymbols =; DFNA12; DFNA8; DFNB21
- | OMIM = 602574
- | ECnumber =
- | Homologene = 3955
- | MGIid = 109575
-  | GeneAtlas_image1 = PBB_GE_TECTA_221296_at_tn.png
- | Function = {{GNF_GO|id=GO:0005201 |text = extracellular matrix structural constituent}} {{GNF_GO|id=GO:0048503 |text = GPI anchor binding}}
- | Component = {{GNF_GO|id=GO:0005578 |text = proteinaceous extracellular matrix}} {{GNF_GO|id=GO:0005615 |text = extracellular space}} {{GNF_GO|id=GO:0016020 |text = membrane}}
- | Process = {{GNF_GO|id=GO:0007160 |text = cell-matrix adhesion}} {{GNF_GO|id=GO:0007605 |text = sensory perception of sound}}
- | Orthologs = {{GNF_Ortholog_box
-    | Hs_EntrezGene = 7007
-    | Hs_Ensembl = ENSG00000109927
-    | Hs_RefseqProtein = NP_005413
-    | Hs_RefseqmRNA = NM_005422
-    | Hs_GenLoc_db =
-    | Hs_GenLoc_chr = 11
-    | Hs_GenLoc_start = 120478585
-    | Hs_GenLoc_end = 120566725
-    | Hs_Uniprot = O75443
-    | Mm_EntrezGene = 21683
-    | Mm_Ensembl = ENSMUSG00000037705
-    | Mm_RefseqmRNA = NM_009347
-    | Mm_RefseqProtein = NP_033373
-    | Mm_GenLoc_db =
-    | Mm_GenLoc_chr = 9
-    | Mm_GenLoc_start = 42080617
-    | Mm_GenLoc_end = 42150924
-    | Mm_Uniprot = O08523
-  }}
-}}
-'''Tectorin alpha''', also known as '''TECTA''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: TECTA tectorin alpha| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7007| accessdate = }}</ref>
 <!-- The PBB_Summary template is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
 {{PBB_Summary
 | section_title =
-| summary_text = The [[tectorial membrane (cochlea)|tectorial membrane]] is an [[extracellular matrix]] of the [[inner ear]] that contacts the [[stereocilia]] bundles of specialized sensory [[hair cell]]s. Sound induces movement of these hair cells relative to the tectorial membrane, deflects the stereocilia, and leads to fluctuations in hair-cell membrane potential, transducing sound into electrical signals. Alpha-tectorin is one of the major noncollagenous components of the tectorial membrane.  Mutations in the TECTA gene have been shown to be responsible for [[autosomal dominant]] [[nonsyndromic deafness|nonsyndromic hearing impairment]] and a recessive form of [[Sensorineural hearing loss|sensorineural pre-lingual non-syndromic deafness]].<ref name="entrez">{{cite web | title = Entrez Gene: TECTA tectorin alpha| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7007| accessdate = }}</ref>
+| summary_text = The [[tectorial membrane (cochlea)|tectorial membrane]] is an [[extracellular matrix]] of the [[inner ear]] that contacts the [[stereocilia]] bundles of specialized sensory [[hair cell]]s. Sound induces movement of these hair cells relative to the tectorial membrane, deflects the stereocilia, and leads to fluctuations in hair-cell membrane potential, transducing sound into electrical signals. Alpha-tectorin is one of the major noncollagenous components of the tectorial membrane.  Mutations in the TECTA gene have been shown to be responsible for [[autosomal dominant]] [[nonsyndromic deafness|nonsyndromic hearing impairment]] and a recessive form of [[Sensorineural hearing loss|sensorineural pre-lingual non-syndromic deafness]].<ref name="entrez" />
 }}
 ==References==
-{{reflist|2}}
+{{reflist}}
 ==Further reading==
 {{refbegin | 2}}
 {{PBB_Further_reading
 | citations =
-*{{cite journal  | author=Van Camp G, Willems PJ, Smith RJ |title=Nonsyndromic hearing impairment: unparalleled heterogeneity. |journal=Am. J. Hum. Genet. |volume=60 |issue= 4 |pages= 758-64 |year= 1997 |pmid= 9106521 |doi=  }}
+*{{cite journal  |vauthors=Van Camp G, Willems PJ, Smith RJ |title=Nonsyndromic hearing impairment: unparalleled heterogeneity |journal=Am. J. Hum. Genet. |volume=60 |issue= 4 |pages= 758–64 |year= 1997 |pmid= 9106521 |doi=  | pmc=1712474  }}
-*{{cite journal  | author=Verhoeven K, Van Camp G, Govaerts PJ, ''et al.'' |title=A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24. |journal=Am. J. Hum. Genet. |volume=60 |issue= 5 |pages= 1168-73 |year= 1997 |pmid= 9150164 |doi=  }}
+*{{cite journal  | author=Verhoeven K |title=A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24 |journal=Am. J. Hum. Genet. |volume=60 |issue= 5 |pages= 1168–73 |year= 1997 |pmid= 9150164 |doi=  | pmc=1712440  |name-list-format=vanc| author2=Van Camp G  | author3=Govaerts PJ  | display-authors=3  | last4=Balemans  | first4=W  | last5=Schatteman  | first5=I  | last6=Verstreken  | first6=M  | last7=Van Laer  | first7=L  | last8=Smith  | first8=RJ  | last9=Brown  | first9=MR  }}
-*{{cite journal  | author=Hughes DC, Legan PK, Steel KP, Richardson GP |title=Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness. |journal=Genomics |volume=48 |issue= 1 |pages= 46-51 |year= 1998 |pmid= 9503015 |doi= 10.1006/geno.1997.5159 }}
+*{{cite journal  | author=Balciuniene J |title=Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family |journal=Am. J. Hum. Genet. |volume=63 |issue= 3 |pages= 786–93 |year= 1998 |pmid= 9718342 |doi=10.1086/302012  | pmc=1377400  |name-list-format=vanc| author2=Dahl N  | author3=Borg E  | display-authors=3  | last4=Samuelsson  | first4=Eva  | last5=Koisti  | first5=Markus J.  | last6=Pettersson  | first6=Ulf  | last7=Jazin  | first7=Elena E.  }}
-*{{cite journal  | author=Verhoeven K, Van Laer L, Kirschhofer K, ''et al.'' |title=Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment. |journal=Nat. Genet. |volume=19 |issue= 1 |pages= 60-2 |year= 1998 |pmid= 9590290 |doi= 10.1038/ng0598-60 }}
+*{{cite journal  | author=Mustapha M |title=An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21 |journal=Hum. Mol. Genet. |volume=8 |issue= 3 |pages= 409–12 |year= 1999 |pmid= 9949200 |doi=10.1093/hmg/8.3.409  |name-list-format=vanc| author2=Weil D  | author3=Chardenoux S  | display-authors=3  | last4=Elias  | first4=S  | last5=El-Zir  | first5=E  | last6=Beckmann  | first6=JS  | last7=Loiselet  | first7=J  | last8=Petit  | first8=C  }}
-*{{cite journal  | author=Balciuniene J, Dahl N, Borg E, ''et al.'' |title=Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family. |journal=Am. J. Hum. Genet. |volume=63 |issue= 3 |pages= 786-93 |year= 1998 |pmid= 9718342 |doi=  }}
+*{{cite journal  | author=Alloisio N |title=Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss |journal=Eur. J. Hum. Genet. |volume=7 |issue= 2 |pages= 255–8 |year= 1999 |pmid= 10196713 |doi= 10.1038/sj.ejhg.5200273  |name-list-format=vanc| author2=Morlé L  | author3=Bozon M  | display-authors=3  | last4=Godet  | first4=Jacqueline  | last5=Verhoeven  | first5=Kristien  | last6=Van Camp  | first6=Guy  | last7=Plauchu  | first7=Henri  | last8=Muller  | first8=Philippe  | last9=Collet  | first9=Lionel }}
-*{{cite journal  | author=Mustapha M, Weil D, Chardenoux S, ''et al.'' |title=An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. |journal=Hum. Mol. Genet. |volume=8 |issue= 3 |pages= 409-12 |year= 1999 |pmid= 9949200 |doi=  }}
+*{{cite journal  | author=Balciuniene J |title=Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypes |journal=Hum. Genet. |volume=105 |issue= 3 |pages= 211–6 |year= 2000 |pmid= 10987647 |doi=10.1007/s004390051091  |name-list-format=vanc| author2=Dahl N  | author3=Jalonen P  | display-authors=3  | last4=Verhoeven  | first4=K.  | last5=Van Camp  | first5=G.  | last6=Borg  | first6=E.  | last7=Pettersson  | first7=U.  | last8=Jazin  | first8=E.E.  }}
-*{{cite journal  | author=Alloisio N, Morlé L, Bozon M, ''et al.'' |title=Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss. |journal=Eur. J. Hum. Genet. |volume=7 |issue= 2 |pages= 255-8 |year= 1999 |pmid= 10196713 |doi= 10.1038/sj.ejhg.5200273 }}
+*{{cite journal  | author=Moreno-Pelayo MA |title=A cysteine substitution in the zona pellucida domain of α-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family |journal=J. Med. Genet. |volume=38 |issue= 5 |pages= E13 |year= 2001 |pmid= 11333869 |doi=10.1136/jmg.38.5.e13  | pmc=1734870  |name-list-format=vanc| author2=del Castillo I  | author3=Villamar M  | display-authors=3  | last4=Romero  | first4=L  | last5=Hernández-Calvín  | first5=FJ  | last6=Herraiz  | first6=C  | last7=Barberá  | first7=R  | last8=Navas  | first8=C  | last9=Moreno  | first9=F  }}
-*{{cite journal  | author=Balciuniene J, Dahl N, Jalonen P, ''et al.'' |title=Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypes. |journal=Hum. Genet. |volume=105 |issue= 3 |pages= 211-6 |year= 2000 |pmid= 10987647 |doi=  }}
+*{{cite journal  | author=Iwasaki S |title=Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss |journal=Arch. Otolaryngol. Head Neck Surg. |volume=128 |issue= 8 |pages= 913–7 |year= 2002 |pmid= 12162770 |doi=  10.1001/archotol.128.8.913|name-list-format=vanc| author2=Harada D  | author3=Usami S  | display-authors=3  | last4=Nagura  | first4=M  | last5=Takeshita  | first5=T  | last6=Hoshino  | first6=T  }}
-*{{cite journal  | author=Moreno-Pelayo MA, del Castillo I, Villamar M, ''et al.'' |title=A cysteine substitution in the zona pellucida domain of alpha-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family. |journal=J. Med. Genet. |volume=38 |issue= 5 |pages= E13 |year= 2001 |pmid= 11333869 |doi=  }}
+*{{cite journal  | author=Naz S |title=Distinctive audiometric profile associated with DFNB21 alleles of TECTA |journal=J. Med. Genet. |volume=40 |issue= 5 |pages= 360–3 |year= 2003 |pmid= 12746400 |doi=10.1136/jmg.40.5.360  | pmc=1735454  |name-list-format=vanc| author2=Alasti F  | author3=Mowjoodi A  | display-authors=3  | last4=Riazuddin  | first4=S  | last5=Sanati  | first5=MH  | last6=Friedman  | first6=TB  | last7=Griffith  | first7=AJ  | last8=Wilcox  | first8=ER  | last9=Riazuddin  | first9=S  }}
-*{{cite journal  | author=Iwasaki S, Harada D, Usami S, ''et al.'' |title=Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss. |journal=Arch. Otolaryngol. Head Neck Surg. |volume=128 |issue= 8 |pages= 913-7 |year= 2002 |pmid= 12162770 |doi=  }}
+*{{cite journal  | author=Pfister M |title=A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations |journal=Cell. Physiol. Biochem. |volume=14 |issue= 4–6 |pages= 369–76 |year= 2005 |pmid= 15319541 |doi= 10.1159/000080347  |name-list-format=vanc| author2=Thiele H  | author3=Van Camp G  | display-authors=3  | last4=Fransen  | first4=Erik  | last5=Apaydin  | first5=Fazil  | last6=Aydin  | first6=Ömer  | last7=Leistenschneider  | first7=Peter  | last8=Devoto  | first8=Marcella  | last9=Zenner  | first9=Hans-Peter }}
-*{{cite journal  | author=Naz S, Alasti F, Mowjoodi A, ''et al.'' |title=Distinctive audiometric profile associated with DFNB21 alleles of TECTA. |journal=J. Med. Genet. |volume=40 |issue= 5 |pages= 360-3 |year= 2003 |pmid= 12746400 |doi=  }}
+*{{cite journal  | author=Plantinga RF |title=A Novel TECTA Mutation in a Dutch DFNA8/12 Family Confirms Genotype–Phenotype Correlation |journal=J. Assoc. Res. Otolaryngol. |volume=7 |issue= 2 |pages= 173–81 |year= 2006 |pmid= 16718611 |doi= 10.1007/s10162-006-0033-z  | pmc=2504577  |name-list-format=vanc| author2=de Brouwer AP  | author3=Huygen PL  | display-authors=3  | last4=Kunst  | first4=Henricus P. M.  | last5=Kremer  | first5=Hannie  | last6=Cremers  | first6=Cor W. R. J. }}
-*{{cite journal  | author=Pfister M, Thiele H, Van Camp G, ''et al.'' |title=A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations. |journal=Cell. Physiol. Biochem. |volume=14 |issue= 4-6 |pages= 369-76 |year= 2005 |pmid= 15319541 |doi= 10.1159/000080347 }}
+*{{cite journal  | author=Plantinga RF |title=Audiological Evaluation of Affected Members from a Dutch DFNA8/12 (TECTA) Family |journal=J. Assoc. Res. Otolaryngol. |volume=8 |issue= 1 |pages= 1–7 |year= 2007 |pmid= 17136632 |doi= 10.1007/s10162-006-0060-9  | pmc=2538417  |name-list-format=vanc| author2=Cremers CW  | author3=Huygen PL  | display-authors=3  | last4=Kunst  | first4=Henricus P. M.  | last5=Bosman  | first5=Arjan J. }}
-*{{cite journal  | author=Plantinga RF, de Brouwer AP, Huygen PL, ''et al.'' |title=A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation. |journal=J. Assoc. Res. Otolaryngol. |volume=7 |issue= 2 |pages= 173-81 |year= 2006 |pmid= 16718611 |doi= 10.1007/s10162-006-0033-z }}
+*{{cite journal  | author=Meyer NC |title=Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus |journal=Am. J. Med. Genet. A |volume=143 |issue= 14 |pages= 1623–9 |year= 2007 |pmid= 17431902 |doi= 10.1002/ajmg.a.31718  |name-list-format=vanc| author2=Alasti F  | author3=Nishimura CJ  | display-authors=3  | last4=Imanirad  | first4=Parisa  | last5=Kahrizi  | first5=Kimia  | last6=Riazalhosseini  | first6=Yasser  | last7=Malekpour  | first7=Mahdi  | last8=Kochakian  | first8=Nafiseh  | last9=Jamali  | first9=Payman }}
-*{{cite journal  | author=Plantinga RF, Cremers CW, Huygen PL, ''et al.'' |title=Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family. |journal=J. Assoc. Res. Otolaryngol. |volume=8 |issue= 1 |pages= 1-7 |year= 2007 |pmid= 17136632 |doi= 10.1007/s10162-006-0060-9 }}
+*{{cite journal  |vauthors=Meyer NC, Nishimura CJ, McMordie S, Smith RJ |title=Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigree |journal=Clin. Genet. |volume=72 |issue= 2 |pages= 130–7 |year= 2007 |pmid= 17661817 |doi= 10.1111/j.1399-0004.2007.00828.x }}
-*{{cite journal  | author=Meyer NC, Alasti F, Nishimura CJ, ''et al.'' |title=Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus. |journal=Am. J. Med. Genet. A |volume=143 |issue= 14 |pages= 1623-9 |year= 2007 |pmid= 17431902 |doi= 10.1002/ajmg.a.31718 }}
-*{{cite journal  | author=Meyer NC, Nishimura CJ, McMordie S, Smith RJ |title=Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigree. |journal=Clin. Genet. |volume=72 |issue= 2 |pages= 130-7 |year= 2007 |pmid= 17661817 |doi= 10.1111/j.1399-0004.2007.00828.x }}
 }}
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TECTA: Difference between revisions

Latest revision as of 22:43, 23 December 2017

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