Human genes for spinocerebellar ataxia type 13
Spinocerebellar ataxia type 13 [DOID:0050963]
An autosomal dominant cerebellar ataxia that is characterized by developmental delay, ataxia, myoclinic jerks, dysarthria, dysphagia and seizure, and has_material_basis_in mutation in the KCNC3 gene.
Synonyms: spinocerebellar ataxia type 13, DOID:0050963