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

dc.contributor.authorHuang, Lijia
dc.contributor.authorWarman-Chardon, Jodi
dc.contributor.authorCarter, Melissa T.
dc.contributor.authorFriend, Kathie L.
dc.contributor.authorDudding, Tracy E.
dc.contributor.authorSchwartzentruber, Jeremy
dc.contributor.authorZou, Ruobing
dc.contributor.authorSchofield, Peter W.
dc.contributor.authorDouglas, Stuart
dc.contributor.authorBulman, Dennis E.
dc.contributor.authorBoycott, Kym M.
dc.date.accessioned2022-04-05T03:25:10Z
dc.date.available2022-04-05T03:25:10Z
dc.date.issued2022-03-29
dc.date.updated2022-04-05T03:25:10Z
dc.identifier.citationOrphanet Journal of Rare Diseases. 2022 Mar 29;17(1):143
dc.identifier.urihttps://doi.org/10.1186/s13023-022-02297-7
dc.identifier.urihttps://doi.org/10.20381/ruor-27653
dc.identifier.urihttp://hdl.handle.net/10393/43437
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dc.titleCorrection to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

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