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Details on Person Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19
| Class:Id | LiteratureReference:375453 |
|---|---|
| _displayName | Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19 |
| _timestamp | 2008-08-29 20:23:02 |
| author | [Person:140432] Seow, HF [Person:352037] Broer, Stefan [Person:352383] Broer, Angelika [Person:375466] Bailey, CG [Person:375469] Potter, SJ [Person:198785] Cavanaugh, JA [Person:375490] Rasko, JE |
| created | [InstanceEdit:375485] D'Eustachio, P, 2008-08-29 20:22:39 |
| journal | Nat Genet |
| modified | [InstanceEdit:375492] D'Eustachio, P, 2008-08-29 20:22:58 |
| pages | 1003-7 |
| pubMedIdentifier | 15286788 |
| title | Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19 |
| volume | 36 |
| year | 2004 |
| (literatureReference) | [Reaction:375473] SLC6A19 cotransports neutral amino acids, Na+ from extracellular region to cytosol [Homo sapiens] [FailedReaction:5659734] Defective SLC6A19 does not cotransport neutral amino acids, Na+ from extracellular region to cytosol [Homo sapiens] |
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No pathways have been reviewed or authored by Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19 (375453)
