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

Huang, LijiaWarman-Chardon, JodiCarter, Melissa T.Friend, Kathie L.Dudding, Tracy E.Schwartzentruber, JeremyZou, RuobingSchofield, Peter W.Douglas, StuartBulman, Dennis E.Boycott, Kym M.2022-04-052022-04-052022-03-29Orphanet Journal of Rare Diseases. 2022 Mar 29;17(1):143https://doi.org/10.1186/s13023-022-02297-7https://doi.org/10.20381/ruor-27653http://hdl.handle.net/10393/43437Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia2022-04-05enThe Author(s)