Visualize Submit Comment

Metadata
ID	DOID:0080062
Name	autosomal recessive spinocerebellar ataxia 13
Definition	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. https://www.ncbi.nlm.nih.gov/pubmed/22901947
Xrefs	MIM:614831
Synonyms	SCAR13 [EXACT]
Parent Relationships	is_a autosomal recessive cerebellar ataxia