Human genes for autosomal recessive spinocerebellar ataxia 24
Autosomal recessive spinocerebellar ataxia 24 [DOID:0111615]
An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in UBA5 on chromosome 3q22.1.
Synonyms: autosomal recessive spinocerebellar ataxia 24, DOID:0111615, SCAR24