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Summary Literature (0)
MIM:618087 - SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND

Xenbase Genes: cacna1g

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0060758 - spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits