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'''Ferredoxin 1-like''' is a [[protein]] that in humans is encoded by the FDX1L [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: Ferredoxin 1-like | url = https://www.ncbi.nlm.nih.gov/gene/112812 }}</ref>
'''Ferredoxin 1-like''' is a [[protein]] that in humans is encoded by the FDX1L [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: Ferredoxin 1-like | url = https://www.ncbi.nlm.nih.gov/gene/112812 }}</ref>
Mutations in '''FDX1L''' cause {{SWL|type=genetic_defect_results_in_disease|target=mitochondrial myopathy|label=mitochondrial myopathy}}.<ref>{{cite journal | vauthors = Spiegel R, Saada A, Halvardson J, Soiferman D, Shaag A, Edvardson S, Horovitz Y, Khayat M, Shalev SA, Feuk L, Elpeleg O | title = Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy | journal = European Journal of Human Genetics | volume = 22 | issue = 7 | pages = 902–6 | date = July 2014 | pmid = 24281368 | doi = 10.1038/ejhg.2013.269 }}</ref>
Mutations in '''FDX1L''' cause {{SWL|type=genetic_defect_results_in_disease|target=mitochondrial myopathy|label=mitochondrial myopathy}}.<ref>{{cite journal | vauthors = Spiegel R, Saada A, Halvardson J, Soiferman D, Shaag A, Edvardson S, Horovitz Y, Khayat M, Shalev SA, Feuk L, Elpeleg O | title = Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy | journal = European Journal of Human Genetics | volume = 22 | issue = 7 | pages = 902–6 | date = July 2014 | pmid = 24281368 | doi = 10.1038/ejhg.2013.269 | pmc = 4060119 }}</ref>
