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Human Disease
autosomal recessive spinocerebellar ataxia 27
- Term ID
- DOID:0111616
- Synonyms
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- SCAR27
- Definition
- An autosomal recessive cerebellar ataxia characterized by adult onset of progressive gait difficulties and other cerebellar signs that has_material_basis_in homozygous or compound heterozygous mutation in the GDAP2 gene on chromosome 1p12. https://www.ncbi.nlm.nih.gov/pubmed/30084953
- References
- Ontology
- Human Disease ( DOID:0111616 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models