Use of Mutant-Specific Ion Channel Characteristics for Risk Stratification of Long QT Syndrome Patients

Author:

Jons Christian1,O-Uchi Jin2,Moss Arthur J.1,Reumann Matthias3,Rice John J.3,Goldenberg Ilan3,Zareba Wojciech1,Wilde Arthur A. M.4,Shimizu Wataru5,Kanters Jorgen K.67,McNitt Scott1,Hofman Nynke8,Robinson Jennifer L.1,Lopes Coeli M. B.2

Affiliation:

1. Cardiology Division, Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.

2. Aab Cardiovascular Research Institute, Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.

3. Functional Genomics and Systems Biology Group, IBM Thomas J. Watson Research Center, Yorktown Heights, NY 10598, USA.

4. Heart Failure Research Centre, Department of Cardiology, Academic Medical Centre, University of Amsterdam, 1105 AZ Amsterdam, Netherlands.

5. National Cardiovascular Center, Suita 565-8565, Japan.

6. Gentofte University Hospital, DK 2820 Copenhagen, Denmark.

7. Danish National Research Foundation Center for Cardiac Arrhythmias, DK 2200 Copenhagen, Denmark.

8. Department of Clinical Genetics, Academic Medical Centre, University of Amsterdam, 1105 AZ, Amsterdam, Netherlands.

Abstract

Mutations that slow the opening of potassium channels in the heart can predict risk for long QT syndrome, a heart arrhythmia that can cause sudden death.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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