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Nature Reviews. Disease Primers|July 18, 2020
Inherited cardiac arrhythmiasPeter J Schwartz, Michael J Ackerman, Charles Antzelevitch, et al.
Heart Rhythm|May 27, 2025
Molecular and functional characterization of DENND3 as a novel regulator of ion channel traffickingShan Gao, Dan Ye, Raquel Neves, et al.
Journal of Cardiovascular Electrophysiology|January 11, 2016
Bileaflet Mitral Valve Prolapse and Risk of Ventricular Dysrhythmias and DeathBenjamin D Nordhues, Konstantinos C Siontis, Christopher G Scott, et al.
Heart Rhythm|July 28, 2009
Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5AArgelia Medeiros-Domingo, Bi-Hua Tan, Pedro Iturralde-Torres, et al.
American Heart Journal|October 27, 2009
Histologic characterization of hypertrophic cardiomyopathy with and without myofilament mutationsChristopher J McLeod, J Martijn Bos, Jeanne L Theis, et al.
Mayo Clinic Proceedings|April 14, 2006
Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: septal morphological features predict the presence of myofilament mutationsJosepha Binder, Steve R Ommen, Bernard J Gersh, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 7, 2014
Reduced junctional Na+/Ca2+-exchanger activity contributes to sarcoplasmic reticulum Ca2+ leak in junctophilin-2-deficient miceWei Wang, Andrew P Landstrom, Qiongling Wang, et al.
JACC. Clinical Electrophysiology|May 19, 2022
Congenital Long QT SyndromeAndrew D Krahn, Zachary Laksman, Raymond W Sy, et al.
Circulation. Cardiovascular Genetics|September 6, 2012
Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndromeJohn R Giudicessi, Jamie D Kapplinger, David J Tester, et al.
Circulation|June 20, 2018
Importance of Variant Interpretation in Whole-Exome Molecular Autopsy: Population-Based Case SeriesGarrett W Shanks, David J Tester, Jaeger P Ackerman, et al.
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