Human genes for spinocerebellar ataxia type 26
Spinocerebellar ataxia type 26 [DOID:0050975]
An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and oculomotor abnormalities, has_material_basis_in mutation in the EEF2 gene.
Synonyms: spinocerebellar ataxia type 26, DOID:0050975