Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
Lijia Huang(University of Ottawa), Kym M. Boycott(Children's Hospital of Eastern Ontario), Jeremy Schwartzentruber(McGill University and Génome Québec Innovation Centre), Dennis E. Bulman(University of Alberta), Ruobing Zou(University of Ottawa), Melissa T. Carter(Agricultural Research Institute of Ontario), Peter W. Schofield(John Hunter Hospital), Tracy Dudding(Hunter Genetics), Jodi Warman‐Chardon(University of Ottawa), K. Friend(South Australia Pathology), Stuart Douglas(University of Ottawa)
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