spinocerebellar ataxia 44

Term ID

DOID:0080286

Synonyms

Definition

An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the GRM1 gene on chromosome 6q24. https://pubmed.ncbi.nlm.nih.gov/28886343/

References

• OMIM:617691

Ontology

Human Disease   ( DOID:0080286 )