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Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
Orphanet Journal of Rare Diseases volume 17, Article number: 143 (2022)
Correction to: Orphanet Journal of Rare Diseases 2012, 7:67 https://doi.org/10.1186/1750-1172-7-67
The original article  unfortunately contained an error to the second author’s name. The article erroneously presented “Jodi” and “Warman” as given names, and “Chardon” as family name. Instead, the author’s given name is “Jodi” and family name is “Warman-Chardon”.
The correct name is included in the author list of this Correction and has already been updated in the original article.
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.
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Huang, L., Warman-Chardon, J., Carter, M.T. et al. Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia. Orphanet J Rare Dis 17, 143 (2022). https://doi.org/10.1186/s13023-022-02297-7