SLC6A19: Difference between revisions
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Revision as of 14:40, 6 September 2012
| solute carrier family 6 (neutral amino acid transporter), member 19 | |
|---|---|
| Identifiers | |
| Symbol | SLC6A19 |
| Entrez | 340024 |
| HUGO | 27960 |
| OMIM | 608893 |
| RefSeq | XM_291120 |
| Other data | |
| Locus | Chr. 5 p15 |
SLC6A19 is a gene associated with Hartnup disease.[1]
References
- ↑ Seow HF, Bröer S, Bröer A; et al. (2004). "Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19". Nat. Genet. 36 (9): 1003–7. doi:10.1038/ng1406. PMID 15286788. Unknown parameter
|month=ignored (help)