The Full Wiki

More info on SLC6A19

SLC6A19: Wikis

Advertisements

Note: Many of our articles have direct quotes from sources you can cite, within the Wikipedia article! This article doesn't yet, but we're working on it! See more info or our list of citable articles.

Encyclopedia

From Wikipedia, the free encyclopedia

SLC6A19
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

  1. ^ Seow HF, Bröer S, Bröer A, et al. (September 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.  
Advertisements

Advertisements






Got something to say? Make a comment.
Your name
Your email address
Message