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

• Lijia Huang,
• Jodi Warman-Chardon,
• Melissa T. Carter,
• Kathie L. Friend,
• Tracy E. Dudding,
• Jeremy Schwartzentruber,
• Ruobing Zou,
• Peter W. Schofield,
• Stuart Douglas,
• Dennis E. Bulman,
• Kym M. Boycott

Affiliations

Lijia Huang

Children’s Hospital of Eastern Ontario Research Institute, University of Ottawa

Jodi Warman-Chardon

Department of Genetics, Children’s Hospital of Eastern Ontario

Melissa T. Carter

Division of Clinical and Metabolic Genetics, Hospital for Sick Children

Kathie L. Friend

Department of Genetic Medicine, Women’s and Children’s Hospital, SA Pathology

Tracy E. Dudding

Hunter Genetics

Jeremy Schwartzentruber

McGill University and Genome Quebec Innovation Centre

Ruobing Zou

Ottawa Hospital Research Institute, University of Ottawa

Peter W. Schofield

Centre for Translational Neuroscience and Mental Health, University of Newcastle

Stuart Douglas

Children’s Hospital of Eastern Ontario Research Institute, University of Ottawa

Dennis E. Bulman

Ottawa Hospital Research Institute, University of Ottawa

Kym M. Boycott

Children’s Hospital of Eastern Ontario Research Institute, University of Ottawa