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MIM:616127 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17
Xenbase Genes: cwf19l1
Human Disease Resource: OMIM
MONDO:0014503 - autosomal recessive spinocerebellar ataxia 17 |
DOID:0080064 - autosomal recessive spinocerebellar ataxia 17 |
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MONDO:0014503 - autosomal recessive spinocerebellar ataxia 17 |
DOID:0080064 - autosomal recessive spinocerebellar ataxia 17 |