KCNE1 G38S polymorphism is not the cause of long QT syndrome

J Electrocardiol. 2016 Mar-Apr;49(2):249-50. doi: 10.1016/j.jelectrocard.2015.12.005. Epub 2015 Dec 12.

Authors

Jørgen K Kanters¹, Morten S Olesen², Michael Christiansen³

Affiliations

¹ Laboratory of Experimental Cardiology, University of Copenhagen, Copenhagen, Denmark. Electronic address: jkanters@sund.ku.dk.
² University of Copenhagen, & Laboratory of Molecular Cardiology, Department of Cardiology, The Heart Centre, Rigshospitalet, Copenhagen, Denmark.
³ Dept. of Clinical Biochemistry, Statens Serum Institut, Copenhagen, Denmark.

PMID: 26781364
DOI: 10.1016/j.jelectrocard.2015.12.005

No abstract available

Publication types

Letter
Comment

MeSH terms

Arrhythmias, Cardiac
Electrocardiography*
Heart Conduction System
Humans
KCNQ1 Potassium Channel
Long QT Syndrome*
Mutation
Polymorphism, Genetic
Potassium Channels, Voltage-Gated / genetics

Substances

KCNQ1 Potassium Channel
Potassium Channels, Voltage-Gated