MW: 122,798 Da. Purity >85% (SDS-PAGE). The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. Defects in this gene are the cause of spinocerebellar ataxia type 2 (SCA2). SCA2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia
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Other Names
[ataxin-2 isoform 1; Ataxin-2; ataxin-2; ataxin 2; Spinocerebellar ataxia type 2 protein homolog]