A KCNQ1 Mutation Causes a High Penetrance for Familial Atrial Fibrillation

Author:

BARTOS DANIEL C.1,ANDERSON JEFFREY B.2,BASTIAENEN RACHEL3,JOHNSON JONATHAN N.4,GOLLOB MICHAEL H.5,TESTER DAVID J.4,BURGESS DON E.1,HOMFRAY TESSA3,BEHR ELIJAH R.3,ACKERMAN MICHAEL J.4,GUICHENEY PASCALE67,DELISLE BRIAN P.1

Affiliation:

1. Department of Physiology, University of Kentucky; Lexington Kentucky USA

2. The Heart Institute, Cincinnati Children's Hospital Medical Center, University of Cincinnati; Cincinnati Ohio USA

3. Cardiovascular Science Research Centre; St. George's University of London; London UK

4. Departments of Medicine; Pediatrics, and Molecular Pharmacology & Experimental Therapeutics/Divisions of Cardiovascular Diseases and Pediatric Cardiology; Mayo Clinic; Rochester Minnesota USA

5. University of Ottawa Heart Institute, Division of Cardiology; Ottawa Ontario Canada

6. INSERM, U956, Hôpital Pitié-Salpêtrière, Fondation ICAN; Paris France

7. UPMC Univ Paris 06, UMR_S956, IFR14; Paris France

Funder

American Heart Association predoctoral award

National Heart Lung and Blood Institute grant

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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