Mutation in the Catalytic Domain of Protein Kinase C γ and Extension of the Phenotype Associated With Spinocerebellar Ataxia Type 14
Open Access
- 1 August 2004
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 61 (8) , 1242-1248
- https://doi.org/10.1001/archneur.61.8.1242
Abstract
Inherited cerebellar ataxias are clinically and genetically heterogeneous. For the autosomal dominant forms, at least 23 loci have been implicated: spinocerebellar ataxia (SCA) 1-8, SCA10-18, SCA19/22, SCA20, SCA21, SCA23, SCA25, and the FGF14 gene–related SCA.1-3Keywords
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