Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
- Resource Type
- article
- Source
- Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-1 (2022)
- Subject
Medicine - Language
- English
- ISSN
- 1750-1172