Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
| dc.contributor.author | Huang, Lijia | |
| dc.contributor.author | Warman-Chardon, Jodi | |
| dc.contributor.author | Carter, Melissa T. | |
| dc.contributor.author | Friend, Kathie L. | |
| dc.contributor.author | Dudding, Tracy E. | |
| dc.contributor.author | Schwartzentruber, Jeremy | |
| dc.contributor.author | Zou, Ruobing | |
| dc.contributor.author | Schofield, Peter W. | |
| dc.contributor.author | Douglas, Stuart | |
| dc.contributor.author | Bulman, Dennis E. | |
| dc.contributor.author | Boycott, Kym M. | |
| dc.date.accessioned | 2022-04-05T03:25:10Z | |
| dc.date.available | 2022-04-05T03:25:10Z | |
| dc.date.issued | 2022-03-29 | |
| dc.date.updated | 2022-04-05T03:25:10Z | |
| dc.identifier.citation | Orphanet Journal of Rare Diseases. 2022 Mar 29;17(1):143 | |
| dc.identifier.uri | https://doi.org/10.1186/s13023-022-02297-7 | |
| dc.identifier.uri | https://doi.org/10.20381/ruor-27653 | |
| dc.identifier.uri | http://hdl.handle.net/10393/43437 | |
| dc.language.rfc3066 | en | |
| dc.rights.holder | The Author(s) | |
| dc.title | Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia |
