Description

The autosomal-dominant spinocerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by slowly progressive cerebellar dysfunction. The most common types of SCAs are 1, 2, 3, 6 and 7 (caused by CAG trinucleotide repeats) and SCA8 (CTA/CTG expansions).

5-7 weeks

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