Gillette / HP / Mayo Clinic’s Sudden Death Genomics Laboratory / Donnelly / Shimizu / Sudden Death Genomics Laboratory / / /
Event
FDA Phase / /
Facility
Hall WJ / Long QT Syndrome Clinic / Mayo Clinic College of Medicine / terminal S2/S3 S5 S5/Pore Pore/S6 / terminal Pore/S6 Family / Sudden Death Genomics Laboratory / /
MedicalCondition
TB / ion channel diseases / torsades de pointes / congenital long QT syndrome / clinical disease / long-QT syndrome / syncope / Durrer D. Ventricular fibrillation / pulmonary thromboembolism / apparent heart disease / appropriate shock / inherited cardiac arrhythmia / cardiac arrest / long QT syndrome / arrhythmia / acquired cardiac arrhythmia / profound neurological injury / hereditary long QT syndrome / sudden cardiac death / cardiac arrhythmias / inherited long QT syndrome / postpartum sudden cardiac death / inherited long-QT syndrome / cardiac arrest Syncope/aborted / KEYWORDS Long QT syndrome / long-QT cardiac arrhythmia / ventricular fibrillation / autosomal dominant long QT syndrome / Zhou Z. Long QT syndrome / idiopathic long QT syndrome / /
NaturalFeature
HERG channel / Keating MT / /
Organization
Doris Duke Charitable Foundation / National Institutes of Health / Heart Rhythm Society / Division of Pediatric Cardiology / Department of Pediatric / Mayo Clinic College of Medicine / S6 Family / Department of Molecular Pharmacology and Experimental Therapeutics / Division of Cardiovascular Disease / Mayo Foundation’s Institutional Review Board / /
Person
Timothy K. Comparison / Syncope Syncope / Bennett V / Andrews M. Influence / J. Ackerman / Van Hare / Michael J. Ackerman / Van Raay / Anant Khositseth / Hada K. Auditory / Wang Z. Increased / /
Position
Rautaharju PM / Fisher / Clinical Scientist Development Award / Porter / /
Heart Rhythm[removed], 60 – 64 www.heartrhythmjournal.com Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome