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Familial Generalised Epilepsy v0.0 | SCN1A |
Bryony Thompson gene: SCN1A was added gene: SCN1A was added to Familial Generalised Epilepsy. Sources: Expert Review Green,GREP Mode of inheritance for gene: SCN1A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SCN1A were set to Epileptic encephalopathy, early infantile, 6 (Dravet syndrome) 607208; Epilepsy, generalized, with febrile seizures plus, type 2 604403 |