Human genes for spinocerebellar ataxia type 4
Spinocerebellar ataxia type 4 [DOID:0050957]
An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, dysarthria and peripheral neuropathy, has_material_basis_in mutation in the SCA4 gene.
Synonyms: spinocerebellar ataxia type 4, DOID:0050957