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Article

SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome features.

Epilepsy & behavior : E&B - 1 Nov 2009

Selmer Kaja Kristine, Lund Caroline, Brandal Kristin, Undlien Dag Erik, Brodtkorb Eylert

Abstract excerpt

Mutations in the SCN1A gene have been identified in a variety of epilepsy phenotypes, from severe encephalopathies such as Dravet syndrome to milder familial forms such as generalized epilepsy with febrile seizures plus. In a previous study, an SCN1A mutation was also identified in a patient with...

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Source

Identifiers

PMID: 19782004
DOI: 10.1016/j.yebeh.2009.08.021

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19782004-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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