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Spinocerebellar Ataxia Type 2 — Gene Therapy & Clinical Trials | FollowGene
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Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2
Prevalence:
1/100000
neurological
Official
·
OMIM:183090
Official
·
ORPHA98756
Cerebellar ataxia caused by CAG repeat expansion in the ATXN2 gene.
Associated Genes
ATXN2
Ataxin 2
Chromosome 12
Autosomal Dominant