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Updated: Apr 14, 2026

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An Interdomain KCNH2 Mutation Produces an Intermediate Long QT Syndrome
Marika L Osterbur1, Renjian Zheng2, Robert Marion3
1Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY.
Human Mutation
|April 28, 2015
Summary
A novel mutation in the human ether-a-go-go related gene (hERG) channel, p.Asp219Val, was identified in a patient with long QT syndrome. This mutation affects cardiac repolarization by altering hERG channel deactivation kinetics.
Area of Science:
- Cardiovascular Genetics
- Molecular Cardiology
- Ion Channel Physiology
Background:
- Hereditary long QT syndrome (LQTS) is a disorder of cardiac repolarization.
- LQTS is often caused by mutations in genes encoding cardiac ion channels, including KCNH2 (hERG).
- The KCNH2 gene (locus LQT2) is crucial for cardiac repolarization.
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