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Article

A new approach to long QT syndrome mutation detection by Sequenom MassARRAY system.

Electrophoresis - 1 May 2010

Allegue Catarina, Gil Rocio, Sanchez-Diz Paula, Torres María, Quintela Inés, Carracedo Angel, Brión María

Abstract excerpt

Congenital long QT syndrome is an inherited cardiac disorder characterized by a prolonged QT interval and polymorphic ventricular arrhythmias that could result in recurrent syncope, seizures or sudden death as the most dramatic event. Until now QT interval mutations have been described in 12 gene...

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Source

Identifiers

PMID: 20486126
DOI: 10.1002/elps.201000022

Genes

KCNH2
KCNQ1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20486126-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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