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Autosomal Recessive Spinocerebellar Ataxia 32
An autosomal recessive cerebellar ataxia characterized by onset of gait ataxia in the second or third decade of life that is caused by homozygous or compound heterozygous mutation in the PRDX3 gene on chromosome 10q26.
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Overview
An autosomal recessive cerebellar ataxia characterized by onset of gait ataxia in the second or third decade of life that is caused by homozygous or compound heterozygous mutation in the PRDX3 gene on chromosome 10q26.
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