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Article

Recent progress in congenital long QT syndrome.

Current opinion in cardiology - 1 May 2010

Lu Jonathan T, Kass Robert S

Abstract excerpt

PURPOSE OF REVIEW: As genetic testing for long QT syndrome (LQTS) has become readily available, important advances are being made in understanding the exact link between ion channel mutation and observed phenotype. This paper reviews recent findings in the literature. RECENT FINDINGS: Congenital LQTS is an important cause of sudden cardiac death. To date, 12 genes have been identified as the cause of congenital...

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Share to Cardiac electrophysiology and arrhythmias
Share to Cardiovascular Effects of Exercise
Share to Death, Sudden, Cardiac

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Ion channel regulation and function

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Share to Long QT Syndrome

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Source

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Identifiers

PMID: 20224391
DOI: 10.1097/HCO.0b013e32833846b3
PMCID: PMC3151313

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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