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Circulation. Genomic and Precision Medicine|February 10, 2021
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical FeaturesAlice Ghidoni, Perry M Elliott, Petros Syrris, et al.
Circulation Research|February 18, 2025
TAX1BP3 Causes TRPV4-Mediated Autosomal Recessive Arrhythmogenic CardiomyopathyRobin M Perelli, Enya R Dewars, Heidi Cope, et al.
Plos One|August 31, 2018
No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathyEdgar T Hoorntje, Anna Posafalvi, Petros Syrris, et al.
Journal of the American College of Cardiology|February 19, 2025
Genes Associated With Hypertrophic Cardiomyopathy: A Reappraisal by the ClinGen Hereditary Cardiovascular Disease Gene Curation Expert PanelSophie Hespe, Amber Waddell, Babken Asatryan, et al.
European Heart Journal|January 25, 2015
Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriersAditya Bhonsale, Judith A Groeneweg, Cynthia A James, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencingChristopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
Circulation|May 5, 2021
Evidence-Based Assessment of Genes in Dilated CardiomyopathyElizabeth Jordan, Laiken Peterson, Tomohiko Ai, et al.
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