SLC6A19

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solute carrier family 6 (neutral amino acid transporter), member 19
Identifiers
SymbolSLC6A19
Entrez340024
HUGO27960
OMIM608893
RefSeqXM_291120
Other data
LocusChr. 5 p15


SLC6A19 is a gene associated with Hartnup disease.[1]

References

  1. 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)

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