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Orphanet Journal of Rare Diseases logoLink to Orphanet Journal of Rare Diseases
. 2022 Mar 29;17:143. doi: 10.1186/s13023-022-02297-7

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

Lijia Huang 1, Jodi Warman-Chardon 2, Melissa T Carter 3, Kathie L Friend 4, Tracy E Dudding 5,6, Jeremy Schwartzentruber 7, Ruobing Zou 8, Peter W Schofield 9, Stuart Douglas 1, Dennis E Bulman 8,10,#, Kym M Boycott 1,2,✉,#
PMCID: PMC8966260  PMID: 35351177

Correction to: Orphanet Journal of Rare Diseases 2012, 7:67 https://doi.org/10.1186/1750-1172-7-67

The original article [1] 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.

Footnotes

Publisher's Note

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Dennis E. Bulman and Kym M. Boycott contributed equally.

Reference


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