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| Ataxia and cerebellar anomalies - narrow panel v0.5 | CWF19L1 |
Ellen McDonagh gene: CWF19L1 was added gene: CWF19L1 was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Green Mode of inheritance for gene: CWF19L1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CWF19L1 were set to 26197978, 25361784, 27016154 Phenotypes for gene: CWF19L1 were set to Spinocerebellar ataxia, autosomal recessive 17, 616127 |
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