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Article

SCN5A mutation associated with acute myocardial infarction.

Legal medicine (Tokyo, Japan) - 1 Apr 2009

Oliva Antonio, Hu Dan, Viskin Sami, Carrier Tabitha, Cordeiro Jonathan M, Barajas-Martinez Hector, Wu Yusheng, Burashnikov Elena, Brugada Ramon, Rosso Rafael, Guerchicoff Alexandra, Pollevick Guido, Pascali Vincenzo L, Antzelevitch Charlie

Abstract excerpt

Ventricular tachycardia and fibrillation (VT/VF) complicating Brugada syndrome, a genetic disorder linked to SCN5A mutations, and VF complicating acute myocardial infarction (AMI) have both been linked to phase 2 reentry. Because of these mechanistic similarities in arrhythmogenesis, we examined the contribution of SCN5A mutations to VT/VF complicating AMI. Nineteen consecutive patients developing VF during AMI...

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Identifiers

PMID: 19345130
DOI: 10.1016/j.legalmed.2009.02.044
PMCID: PMC2813686

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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