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J Cardiovasc Electrophysiol. 2000 Dec;11(12):1413-8.

Long QT syndrome: cellular basis and arrhythmia mechanism in LQT2.

Author information

1
Department of Medicine, University of Wisconsin, Madison, USA. ctj@medicine.wisc.edu

Abstract

LQT2 is one form of the congenital long QT syndrome. It results from mutations in the human ether-a-go-go-related gene (HERG), and more than 80 mutations, usually causing single amino acid substitutions in the HERG protein, are known. HERG encodes the ion channel pore-forming subunit protein for the rapidly activating delayed rectifier K+ channel (I(Kr)) in the heart. This review summarizes current findings about mutations causing LQT2, the mechanisms by which mutations may cause the clinical phenotype of a reduction in I(Kr) and a prolonged QT interval, and how this may be involved in the generation of ventricular arrhythmias.

PMID:
11196567
[Indexed for MEDLINE]

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