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Article

Focal Seizures in Patients With SCN1A Mutations.

Journal of child neurology - 1 Feb 2017

McDonald Christopher L, Saneto Russell P, Carmant Lionel, Sotero de Menezes Márcio A

Abstract excerpt

The SCN1A gene has been implicated in the etiology of various forms of epilepsy. New research has linked this gene to specific types of epilepsy, all of which present in infancy or early childhood. This study examines the time course and pathology of pediatric patients who have a mutation in the SCN1A gene in order to open a discussion regarding the key trends of this form of epilepsy as well as important...

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Source

Identifiers

PMID: 27777328
DOI: 10.1177/0883073816672379

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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