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Spinocerebellar Ataxia Type 1 — Gene Therapy & Clinical Trials | FollowGene
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Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1
Prevalence:
1/100000
neurological
Official
·
OMIM:164400
Official
·
ORPHA98755
Cerebellar ataxia caused by CAG repeat expansion in the ATXN1 gene.
Associated Genes
ATXN1
Ataxin 1
Chromosome 6
Autosomal Dominant