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Paper Details

Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locus.
Am J Med Genet A
14
2015
5'-AMP, 5'-AMP-activated protein kinase subunit -2, E1885K, KCNE2, Long QT syndrome, MYH6, MYH6 p, MYH6 p., MYH6 variants, PRKAG2, WPW, Wolff-Parkinson-White (WPW) syndrome, Wolff-Parkinson-White syndrome, atrial septal defects, cardiomyopathies, disease locus, p.E1885K, patients, sick sinus syndrome, sudden cardiac death, supraventricular tachycardia
Author NameAffiliation
Nori MatsunamiUniversity of Utah School of Medicine
Lindsay MeyersUniversity of Utah School of Medicine
H Joseph YostUniversity of Utah School of Medicine
Mark YandellUniversity of Utah School of Medicine
Mark YandellUSTAR Center for Genetic Discovery, University of Iowa
Mark YandellUniversity of Utah School of Medicine
Mark YandellUSTAR Center for Genetic Discovery, University of Iowa
Mark F LeppertUniversity of Utah School of Medicine
Mark F LeppertUniversity of Utah School of Medicine
Martin Tristani-FirouziUniversity of Utah School of Medicine
Martin Tristani-FirouziNora Eccles Cardiovascular Research and Training Institute
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Release 1.2