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Article

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.

Brain : a journal of neurology - 1 Aug 2012

Brunklaus A, Ellis R, Reavey E, Forbes G H, Zuberi S M

Abstract excerpt

Dravet syndrome is a severe infantile onset epileptic encephalopathy associated with mutations in the sodium channel alpha 1 subunit gene SCN1A. To date no large studies have systematically examined the prognostic, clinical and demographic features of the disease. We prospectively collected data...

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Identifiers

PMID: 22719002
DOI: 10.1093/brain/aws151

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22719002-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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