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Article

Development of a high resolution melting method for the detection of genetic variations in Long QT Syndrome.

Clinica chimica acta; international journal of clinical chemistry - 14 Jan 2011

Millat Gilles, Chanavat Valérie, Créhalet Hervé, Rousson Robert

Abstract excerpt

BACKGROUND: Inherited Long QT Syndrome (LQTS) is a cardiac channelopathy associated with a high risk of sudden death. The prevalence has been estimated at close to 1:2000. Due to large cohorts to investigate, the size of the 3 prevalent mutated genes, and the presence of a large spectrum of priva...

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Source

Identifiers

PMID: 20851114
DOI: 10.1016/j.cca.2010.09.013

Genes

KCNH2
KCNQ1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20851114-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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