Impaired ion channel function related to a common KCNQ1 mutation — Implications for risk stratification in long QT syndrome 1
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference49 articles.
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4. Mutations in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events: implications for mutation-specific response to β-blocker therapy in type 1 long-QT syndrome;Barsheshet;Circulation,2012
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1. Long-QT founder variant T309I-Kv7.1 with dominant negative pattern may predispose delayed afterdepolarizations under β-adrenergic stimulation;Scientific Reports;2021-02-11
2. Predicting the Functional Impact of KCNQ1 Variants of Unknown Significance;Circulation: Cardiovascular Genetics;2017-10
3. Molecular Pathophysiology of Congenital Long QT Syndrome;Physiological Reviews;2017-01
4. Inherited Arrhythmias: Of Channels, Currents, and Swimming;Biophysical Journal;2016-03
5. Conformational changes of an ion-channel during gating and emerging electrophysiologic properties: Application of a computational approach to cardiac Kv7.1;Progress in Biophysics and Molecular Biology;2016-01
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