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Article

Novel brugada SCN5A mutation leading to ST segment elevation in the inferior or the right precordial leads.

Journal of cardiovascular electrophysiology - 1 Feb 2003

Potet Franck, Mabo Philippe, Le Coq Guillaume, Probst Vincent, Schott Jean-Jacques, Airaud Fabrice, Guihard Gilles, Daubert Jean-Claude, Escande Denis, Le Marec Hervé

Abstract excerpt

Mutations in the SCN5A gene can lead to the Brugada syndrome, a genetically inherited form of idiopathic ventricular fibrillation that has a characteristic ECG phenotype usually restricted to precordial leads V1-V3. We identified a novel G752R SCN5A missense mutation leading to various degrees of the Brugada ECG phenotype in members of a French family. In the proband, the G752R mutation produced ST segment...

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Identifiers

PMID: 12693506
DOI: 10.1046/j.1540-8167.2003.02382.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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