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Article

Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy

20 Jul 2012

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Share to Epilepsy research and treatment
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23195492
DOI: 10.1016/j.eplepsyres.2012.06.006

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Related research

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Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsyPMID 23195492Read ↗

The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: a population-based study from 2004 to 2009.Semantic proximity Read ↗

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SCN1A Gene Mutations in Indian Children With Epilepsy: Single Center Experience.Semantic proximity Read ↗

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SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations.Semantic proximity Read ↗

Clinical and Genetic Features of Dravet Syndrome: A Prime Example of the Role of Precision Medicine in Genetic EpilepsySemantic proximity Read ↗

Impact of variant subtype on electro-clinical phenotype of Dravet syndrome- a South Indian cohort study.Semantic proximity Read ↗

Genetic exploration of Dravet syndrome: two case report.Semantic proximity Read ↗

Dravet syndrome and its mimics: Beyond SCN1A.Semantic proximity Read ↗

Determination of SCN1A genetic variants in Mexican patients with refractory epilepsy and Dravet syndrome.Semantic proximity Read ↗

SCN1A gain of function effects in Dravet syndrome: Insights into clinical phenotypes and therapeutic implicationsSemantic proximity Read ↗

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