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Article

De novo mutation in the SCN5A gene associated with early onset of sudden infant death.

Circulation - 4 Sept 2001

Wedekind H, Smits J P, Schulze-Bahr E, Arnold R, Veldkamp M W, Bajanowski T, Borggrefe M, Brinkmann B, Warnecke I, Funke H, Bhuiyan Z A, Wilde A A, Breithardt G, Haverkamp W

Abstract excerpt

BACKGROUND: Congenital long QT syndrome (LQTS), a cardiac ion channel disease, is an important cause of sudden cardiac death. Prolongation of the QT interval has recently been associated with sudden infant death syndrome, which is the leading cause of death among infants between 1 week and 1 year...

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Source

Identifiers

PMID: 11535573
DOI: 10.1161/hc3501.095361

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-11535573-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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