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

Fichiers

13023_2022_Article_2297.pdf (552.69 KB)

Date

Authors

Warman-Chardon, Jodi

Carter, Melissa T.

Friend, Kathie L.

Dudding, Tracy E.

Schwartzentruber, Jeremy

Schofield, Peter W.

Douglas, Stuart

Bulman, Dennis E.

Citation

Orphanet Journal of Rare Diseases. 2022 Mar 29;17(1):143

URI

https://doi.org/10.1186/s13023-022-02297-7
https://doi.org/10.20381/ruor-27653
http://hdl.handle.net/10393/43437

Collections

Publications par les auteurs d'uOttawa publiés par BioMed Central // uOttawa authored publications from BioMed Central

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