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Long QT syndrome: from channels to cardiac arrhythmias
Arthur J. Moss, Robert S. Kass
Arthur J. Moss, Robert S. Kass
Published August 1, 2005
Citation Information: J Clin Invest. 2005;115(8):2018-2024. https://doi.org/10.1172/JCI25537.
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Review Series

Long QT syndrome: from channels to cardiac arrhythmias

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Abstract

Long QT syndrome, a rare genetic disorder associated with life-threatening arrhythmias, has provided a wealth of information about fundamental mechanisms underlying human cardiac electrophysiology that has come about because of truly collaborative interactions between clinical and basic scientists. Our understanding of the mechanisms that control the critical plateau and repolarization phases of the human ventricular action potential has been raised to new levels through these studies, which have clarified the manner in which both potassium and sodium channels regulate this critical period of electrical activity.

Authors

Arthur J. Moss, Robert S. Kass

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