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Spinocerebellar Ataxia with Axonal Neuropathy 1
A nervous system disease characterized by autosomal recessive inheritance of spinocerebellar ataxia and peripheral neuropathy that is caused by homozygosity for a mutation in the TDP1 gene on chromosome 14q32.11.
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Overview
A nervous system disease characterized by autosomal recessive inheritance of spinocerebellar ataxia and peripheral neuropathy that is caused by homozygosity for a mutation in the TDP1 gene on chromosome 14q32.11.
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