Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

Affiliations

• ¹ Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.
• ² Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.
• ³ Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, ON, Canada.
• ⁴ Department of Genetic Medicine, Women's and Children's Hospital, SA Pathology, North Adelaide, Australia.
• ⁵ Hunter Genetics, Warratah, NSW, Australia.
• ⁶ University of Newcastle, Newcastle, NSW, Australia.
• ⁷ McGill University and Genome Quebec Innovation Centre, Montréal, QC, Canada.
• ⁸ Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada.
• ⁹ Centre for Translational Neuroscience and Mental Health, University of Newcastle, Newcastle, NSW, Australia.
• ¹⁰ Division of Neurology, Ottawa Hospital and University of Ottawa, Ottawa, ON, Canada.
• ¹¹ Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada. kboycott@cheo.on.ca.
• ¹² Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada. kboycott@cheo.on.ca.