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Browsing by Author Bailey, Charles

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Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19

Author(s)Seow, Heng; Broer, Stefan; Broer, Angelika, et al
TypeJournal article
Date Published2004
Date Created-

Persistence of the Common Hartnup disease D173N Allele in populations of European origin

Author(s)Azmanov, Dimitar; Rodgers, Helen; Auray-Blais, Christiane, et al
TypeJournal article
Date Published2007
Date Created-

Renal imino acid and glycine transport system ontogeny and involvement in developmental iminoglycinuria

Author(s)Vanslambrouck, Jessica M.; Broer, Angelika; Thavyogarajah, Thuvaraka, et al
TypeJournal article
Date Published2010
Date Created-
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