Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop ofHERG
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference6 articles.
1. MiRP1 Forms IKr Potassium Channels with HERG and Is Associated with Cardiac Arrhythmia
2. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
3. Mutations in the hminK gene cause long QT syndrome and suppress lKs function
4. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
5. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
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