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MIM:607317 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4
Xenbase Genes: vps13d
Human Disease Resource: MIM
MONDO:0011811 - autosomal recessive cerebellar ataxia-saccadic intrusion syndrome |
DOID:0111611 - autosomal recessive spinocerebellar ataxia 4 |