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Ataxia and cerebellar anomalies - narrow panel v0.5 | ZNF592 |
Ellen McDonagh gene: ZNF592 was added gene: ZNF592 was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Red Mode of inheritance for gene: ZNF592 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ZNF592 were set to Spinocerebellar ataxia, autosomal recessive 5 |