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资源简介：
genesets as reported in the study by **Koko et al. EBioMedicine 2021**
应用场景：
创建时间：
2023-05-03
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Data_Sheet_1_SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis.ZIP
Background:SCN1A is one of the most common epilepsy genes. About 80% of SCN1A gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic encephalopathy. More than 1,800 mu
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