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Article

Mutation analysis for the detection of long QT-syndrome (LQTS) associated SNPs.

International journal of legal medicine - 1 Mar 2017

J Edelmann, T Dobosz, M Sobieszczanska, M Kawecka-Negrusz, J Dreßler, M Nastainczyk-Wulf

Abstract excerpt

Congenital long QT-syndrome (LQTS) is an inherited cardiac arrhythmia, which is characterized by a prolonged QT interval which predisposes to sudden cardiac death due to ventricular arrhythmias. The altered functions are based on different mutations in LQTS-associated genes. In this study, we performed a mutation analysis for the detection of 125 LQTS-associated single nucleotide polymorphisms (SNPs) focused on...

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Source

Identifiers

PMID: 27613431
DOI: 10.1007/s00414-016-1446-9

Genes

KCNH2
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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