Metadata | |
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ID | DOID:0080064 |
Name | autosomal recessive spinocerebellar ataxia 17 |
Definition | An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CWF19L1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/26197978 |
Xrefs | |
Synonyms |
SCAR17 [EXACT] |
Parent Relationships |