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Article

Long QT molecular autopsy in sudden infant death syndrome.

Archives of disease in childhood - 1 Jul 2014

Glengarry Joanna Moira, Crawford Jackie, Morrow Paul Lowell, Stables Simon Robert, Love Donald Roy, Skinner Jonathan Robert

Abstract excerpt

OBJECTIVE: To describe experience of long QT (LQT) molecular autopsy in sudden infant death syndrome (SIDS). DESIGN: Descriptive audit from two distinct periods: (1) A prospective, population-based series between 2006 and 2008 ('unselected'). (2) Before and after 2006-2008, with testing guided by a cardiac genetic service ('selected'). LQT genes 1, 2, 3, 5, 6 and 7 were sequenced. Next of kin were offered cardiac...

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Source

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Identifiers

PMID: 24596401
DOI: 10.1136/archdischild-2013-305331
PMCID: PMC4078670

Genes

KCNH2
KCNQ1

Variants

Provenance

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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