Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder
Robert Kleta(National Institutes of Health), Elisa Romeo(University of Zurich), Zorica Ristic(University of Zurich), Toshihiro Ohura(Tohoku University), Caroline Stuart(National Institutes of Health), Mauricio Arcos‐Burgos(National Institutes of Health), Mital H. Dave(University of Zurich), Carsten A. Wagner(University of Zurich), Simone R M Camargo(University of Zurich), Sumiko Inoue(Kyoto University), Norio Matsuura(Kyoto University), Amanda Helip‐Wooley(National Institutes of Health), Detlef Böckenhauer(Yale University), Richard Warth(University of Regensburg), Isa Bernardini(National Institutes of Health), Gepke Visser(Wilhelmina Children's Hospital), Thomas Eggermann(Universitätsklinikum Aachen), Philip Lee(National Hospital for Neurology and Neurosurgery), Arthit Chairoungdua(Kyorin University), Promsuk Jutabha(Kyorin University), Ellappan Babu(Kyorin University), Sirinun Nilwarangkoon(Kyorin University), Naohiko Anzai(Kyorin University), Yoshikatsu Kanai(Kyorin University), François Verrey(University of Zurich), William A. Gahl(National Institutes of Health), Akio Koizumi(Kyoto University)
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