The role of the neutral amino acid transporter B0AT1 (SLC6A19) in Hartnup disorder and protein nutrition
Author:
Publisher
Wiley
Subject
Cell Biology,Clinical Biochemistry,Genetics,Molecular Biology,Biochemistry
Reference67 articles.
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4. Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder;Kleta;Nat. Genet.,2004
5. Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19;Seow;Nat. Genet.,2004
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