Human genes for spinocerebellar ataxia type 35
Spinocerebellar ataxia type 35 [DOID:0050982]
An autosomal dominant cerebellar ataxia that is characterized by a slowly progressive ataxia, tremor, dysarthria and hyperreflexia, has_material_basis_in mutation in the TGM6 gene.
Synonyms: spinocerebellar ataxia type 35, DOID:0050982