Mutation in the KCNQ1 Gene Leading to the Short QT-Interval Syndrome

By C. Bellocq, A. V. van Ginneken, C. Bezzina, M. Alders, D. Escande, M. Mannens, I. Baró, A. Wilde. Circulation, 2004

635 citations recorded by the source corpus.

Subfields: Cardiology and Cardiovascular Medicine, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/05fb8948bb9653a68ef77a25ed8d90f19e0050b9

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Cardiology and Cardiovascular Medicine

1. Geoffrey W. Abbott
2. R. Kass
3. J. Nerbonne

In Molecular Biology

1. Geoffrey W. Abbott
2. R. Kass
3. J. Nerbonne

Citations in the corpus

• Biology of the KCNQ1 Potassium Channel (2014, background): “KCNQ1 gain-of-function mutations have also been associated with the rarer but equally dangerous Short QT Syndrome, in which early ventricular myocyte repolarization triggers fatal arrhythmias [74], and also with familial atrial fibrillation [75].”
• Molecular physiology of cardiac repolarization. (2005, background): “KCNE1, produces IKs-like currents with markedly altered activation kinetics and voltage-dependent properties (46)”