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| Ataxia and cerebellar anomalies - narrow panel v0.5 | FRMD4A |
Ellen McDonagh gene: FRMD4A was added gene: FRMD4A was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Red Mode of inheritance for gene: FRMD4A was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FRMD4A were set to 25388005 Phenotypes for gene: FRMD4A were set to Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia, 616819 |
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