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Human Disease

autosomal recessive spinocerebellar ataxia 27

Term ID
DOID:0111616
Synonyms
  • 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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models