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Article

Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome

24 Sept 2009

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 19783390
DOI: 10.1016/j.braindev.2009.08.009

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Missense mutation of the sodium channel gene SCN2A causes Dravet syndromePMID 19783390Read ↗

[Analysis of SCN1A gene variants among patients with Dravet syndrome].Semantic proximity Read ↗

Clinical spectrum of SCN2A mutationsSemantic proximity Read ↗

[Genetic and phenotypic characteristics of SCN1A mutations in Dravet syndrome].Semantic proximity Read ↗

Hereditary dysfunction of voltage-gated sodium channels: from clinical phenotype to molecular mechanisms.Semantic proximity Read ↗

[Genetics Analysis of patients with Dravet syndrome due to mosaicism variation of paternal SCN1A gene].Semantic proximity Read ↗

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

Inherited SCN1A missense mutation in a Dravet Syndrome family: Neuropathological correlation, family screening and implications for adult carriers.Semantic proximity Read ↗

Novel SCN1A variants in Dravet syndrome and evaluating a wide approach of patient selection.Semantic proximity Read ↗

Voltage-gated sodium channels: action players with many faces.Semantic proximity Read ↗

Spectrum of <i>SCN1A</i> gene mutations associated with Dravet syndrome: analysis of 333 patientsSemantic proximity Read ↗

De novo R853Q mutation of SCN2A gene and West syndrome.Semantic proximity Read ↗

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.Semantic proximity Read ↗

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