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Article

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

JAMA - 14 Nov 2001

Ackerman M J, Siu B L, Sturner W Q, Tester D J, Valdivia C R, Makielski J C, Towbin J A

Abstract excerpt

CONTEXT: Fatal arrhythmias from occult long QT syndrome may be responsible for some cases of sudden infant death syndrome (SIDS). Because patients who have long QT syndrome with sodium channel gene (SCN5A) defects have an increased frequency of cardiac events during sleep, and a recent case is reported of a sporadic SCN5A mutation in an infant with near SIDS, SCN5A has emerged as the leading candidate ion channel...

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Identifiers

PMID: 11710892
DOI: 10.1001/jama.286.18.2264

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

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