Functional Invalidation of Putative Sudden Infant Death Syndrome–Associated Variants in the KCNH2 -Encoded Kv11.1 Channel

Author:

Smith Jennifer L.1,Tester David J.2,Hall Allison R.1,Burgess Don E.1,Hsu Chun-Chun3,Claude Elayi Samy4,Anderson Corey L.5,January Craig T.5,Luo Jonathan Z.6,Hartzel Dustin N.6,Mirshahi Uyenlinh L.6,Murray Michael F.6,Mirshahi Tooraj6,Ackerman Michael J.2,Delisle Brian P.1

Affiliation:

1. Department of Physiology, Cardiovascular Research Center, Center for Muscle Biology, University of Kentucky, Lexington (J.L.S., A.R.H., D.E.B., B.P.D.).

2. Departments of Cardiovascular Diseases, Pediatrics, and Molecular Pharmacology & Experimental Therapeutics, Divisions of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN (D.J.T., M.J.A.).

3. School of Respiratory Therapy, College of Medicine, Taipei Medical University, Taiwan (C.-C.H.).

4. University of Kentucky, Gill Heart Institute and VAMC, Cardiology, Lexington (S.C.E.).

5. Cellular and Molecular Arrhythmias Research Program, Department of Medicine, University of Wisconsin, Madison (C.L.A., C.T.J.).

6. Department of Molecular and Functional Genomics and Genomic Medicine Institute, Geisinger Clinic, Danville, PA (J.Z.L., D.N.H., U.L.M., M.F.M., T.M.).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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