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Summary Literature (0)
MIM:617633 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26

Xenbase Genes: xrcc1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0033116 - spinocerebellar ataxia, autosomal recessive 26

Disease Ontology (DO):
DOID:0080260 - autosomal recessive spinocerebellar ataxia 26