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| Ataxia - paediatric v0.0 | CWF19L1 |
Bryony Thompson gene: CWF19L1 was added gene: CWF19L1 was added to Ataxia - paediatric_RMH. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: CWF19L1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CWF19L1 were set to Spinocerebellar ataxia, autosomal recessive 17, 616127; Autosomal recessive spinocerebellar ataxia type 17, 616127 |
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