Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19.
Seow HF; Bröer S; Bröer A; Bailey CG; Potter SJ; Cavanaugh JA; Rasko JE; Nature Genetics, 2004, vol. 36, issue 9, p 1003, ISSN 10614036. ISBN 10614036.

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