A recombinant N-terminal domain fully restores deactivation gating in N-truncated and long QT syndrome mutant hERG potassium channels
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference42 articles.
1. A family of potassium channel genes related to eag in Drosophila and mammals.
2. A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel
3. HERG, a Human Inward Rectifier in the Voltage-Gated Potassium Channel Family
4. Two components of cardiac delayed rectifier K+ current. Differential sensitivity to block by class III antiarrhythmic agents.
5. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
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