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Article

Gene sequencing in neonates and infants with the long QT syndrome.

Genetic testing - 1 Jan 2005

Shim Sung Han, Ito Masamichi, Maher Thomas, Milunsky Aubrey

Abstract excerpt

The objective was to analyze the clinical and molecular findings in a cohort of neonates and infants with the autosomal dominant long QT syndrome (LQTS). Those affected face a high risk of ventricular arrhythmia resulting in syncope, seizure or sudden death. Blood samples submitted for molecular diagnostic studies on 7 infants were subject to DNA extraction and mutation analysis of 18 selected exons in 5 LQTS...

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Source

Identifiers

PMID: 16379539
DOI: 10.1089/gte.2005.9.281

Genes

KCNQ1

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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