Long QT and ventricular arrhythmias in transgenic mice expressing the N terminus and first transmembrane segment of a voltage-gated potassium channel
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference36 articles.
1. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
2. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
3. A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel
4. HERG, a Human Inward Rectifier in the Voltage-Gated Potassium Channel Family
5. Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel
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