Human genes for spinocerebellar ataxia type 14
Spinocerebellar ataxia type 14 [DOID:0050964]
An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the PRKCG gene.
Synonyms: spinocerebellar ataxia type 14, DOID:0050964