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Statements

Subject Item

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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 GDAP2 on chromosome 1p12.

obo:hasDbXref

url:https://www.ncbi.nlm.nih.gov/pubmed/30084953