Human genes for autosomal recessive spinocerebellar ataxia 13
Autosomal recessive spinocerebellar ataxia 13 [DOID:0080062]
An autosomal recessive cerebellar ataxia that is characterized by delayed psychomotor development beginning in infancy and that has_material_basis_in homozygous mutation in the GRM1 gene on chromosome 6q24.
Synonyms: autosomal recessive spinocerebellar ataxia 13, DOID:0080062