Common variants in KCNN3 are associated with lone atrial fibrillation

Patrick T Ellinor,Kathryn L Lunetta,Nicole L Glazer,Arne Pfeufer,Alvaro Alonso,Mina K Chung,Moritz F Sinner,Paul I W de Bakker,Martina Mueller,Steven A Lubitz,Ervin Fox,Dawood Darbar,Nicholas L Smith,Jonathan D Smith,Renate B Schnabel,Elsayed Z Soliman,Kenneth M Rice,David R Van Wagoner, Britt-M Beckmann,Charlotte van Noord,Ke Wang,Georg B Ehret,Jerome I Rotter,Stanley L Hazen,Gerhard Steinbeck,Albert V Smith,Lenore J Launer,Tamara B Harris,Seiko Makino,Mari Nelis,David J Milan,Siegfried Perz,Tõnu Esko,Anna Köttgen,Susanne Moebus,Christopher Newton-Cheh,Man Li,Stefan Möhlenkamp,Thomas J Wang,W H Linda Kao,Ramachandran S Vasan,Markus M Nöthen,Calum A MacRae,Bruno H Ch Stricker,Albert Hofman, André G Uitterlinden,Daniel Levy,Eric Boerwinkle,Andres Metspalu,Eric J Topol,Aravinda Chakravarti,Vilmundur Gudnason,Bruce M Psaty,Dan M Roden,Thomas Meitinger,H-Erich Wichmann,Jacqueline C M Witteman,John Barnard,Dan E Arking,Emelia J Benjamin,Susan R Heckbert,Stefan Kääb

Nature Genetics（2010）

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摘要

Patrick Ellinor and colleagues report a genome-wide association study identifying variants in KCNN3 associated to lone atrial fibrillation.

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关键词

Atrial fibrillation,Genetic predisposition to disease,Genetic variation,Genome-wide association studies,Biomedicine,general,Human Genetics,Cancer Research,Agriculture,Gene Function,Animal Genetics and Genomics

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