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MIM:604326 - SPINOCEREBELLAR ATAXIA 12; SCA12
Xenbase Genes: ppp2r2b
Human Disease Resource: MIM
MONDO:0011439 - spinocerebellar ataxia type 12 |
DOID:0050962 - spinocerebellar ataxia type 12 |
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MONDO:0011439 - spinocerebellar ataxia type 12 |
DOID:0050962 - spinocerebellar ataxia type 12 |