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Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3
rare
Identifiers
MONDO:0020770
OMIM:618387
Causal genes
COA7
Part of
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy
Also known as
SCAN3
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