Spinocerebellar Ataxia Type 23 (SCA23): A Rare Cause of SCA in the Americas
Victor Monteiro Dias Saadeh, Daniel Nassif, Luiz Felipe Vasconcellos
The Cerebellum, 2026
Abstract
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References
- Prodynorphin Mutations Cause the Neurodegenerative Disorder Spinocerebellar Ataxia Type 23 2010
- Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3 2004
- Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia 2012
- The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene 2015
- Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population 2012