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

Citation

Seow, H, Broer, S, Broer, A et al 2004, 'Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19', Nature Genetics, vol. 36, no. 9, pp. 1003-1007.

Year

2004

Fields of Research

  • Receptors And Membrane Biology
  • Tree Nutrition And Physiology

Updated:  30 November 2022 / Responsible Officer:  Director (Research Services Division) / Page Contact:  Researchers