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

Lijia Huang¹, Jodi Warman-Chardon², Melissa T Carter³, Kathie L Friend⁴, Tracy E Dudding^{5

6}, Jeremy Schwartzentruber⁷, Ruobing Zou⁸, Peter W Schofield⁹, Stuart Douglas¹, Dennis E Bulman^#^{8

10}, Kym M Boycott^#^{11

12}

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.

^# Contributed equally.

Published Erratum

Lijia Huang et al. Orphanet J Rare Dis. 2022.

. 2022 Mar 29;17(1):143.

doi: 10.1186/s13023-022-02297-7.

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.

^# Contributed equally.

No abstract available

Erratum for

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.
Huang L, Chardon JW, Carter MT, Friend KL, Dudding TE, Schwartzentruber J, Zou R, Schofield PW, Douglas S, Bulman DE, Boycott KM. Huang L, et al. Orphanet J Rare Dis. 2012 Sep 17;7:67. doi: 10.1186/1750-1172-7-67. Orphanet J Rare Dis. 2012. PMID: 22986007 Free PMC article.

1. Huang, et al. Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia. Orphanet J Rare Dis. 2012;7:67. http://www.ojrd.com/content/7/1/67. - PMC - PubMed