## Abstract Autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurological disorders. Point mutations in the gene encoding protein kinase Cγ (__PRKCG__) are responsible for spinocerebellar ataxia 14 (SCA14). We screened for mutations in the __PRKCG__ gene, in a large series
✦ LIBER ✦
A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14
✍ Scribed by Takehiro Ueda, Tsuneyoshi Seki, Kimitaka Katanazaka…
- Book ID
- 120898569
- Publisher
- Springer
- Year
- 2013
- Tongue
- English
- Weight
- 270 KB
- Volume
- 260
- Category
- Article
- ISSN
- 0340-5354
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