Partial restoration of the long QT syndrome associated KCNQ1 A341V mutant by the KCNE1 β-subunit
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics
Reference40 articles.
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2. Molecular and cellular mechanisms of cardiac arrhythmias;Keating;Cell,2001
3. The KCNQ1 potassium channel: from gene to physiological function;Jespersen;Physiology (Bethesda, Md.),2005
4. KCNE regulation of KvLQT1 channels: structure-function correlates;Melman;Trends Cardiovasc. Med.,2002
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1. Targeting the I Ks Channel PKA Phosphorylation Axis to Restore Its Function in High-Risk LQT1 Variants;Circulation Research;2024-09-13
2. Estimating the probability of early afterdepolarizations and predicting arrhythmic risk associated with long QT syndrome type 1 mutations;Biophysical Journal;2023-10
3. Clinical and Genetic Characteristics of Congenital Long QT Syndrome;Russian Journal of Genetics;2022-10
4. Age-dependent transition from islet insulin hypersecretion to hyposecretion in mice with the long QT-syndrome loss-of-function mutation Kcnq1-A340V;Scientific Reports;2021-06-10
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