Arrhythmogenic cardiomyopathy phenotype associated with the pathogenic founder variant c.1211dup in PKP2
Thomas Bos(Leiden University), Daniela Q.C.M. Barge‐Schaapveld(Leiden University), Arjan C. Houweling(ERN GUARD-Heart), Marja W. Wessels(Erasmus MC), J. Peter van Tintelen(Utrecht University), Anneline S.J.M. te Riele(Utrecht University), Y M Hoedemakers(Radboud University Nijmegen), Sebastiaan R.D. Piers(Leiden University Medical Center), Tamara T. Koopmann(University of Washington), Laurens P. Bosman(Heidelberg University)
Cited by 0
Related Papers
2023 ESC Guidelines for the management of cardiomyopathies
|European Heart Journal|2023|2.3k
Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers
|Journal of the American College of Cardiology|2012|519
Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
|Nature Communications|2018|395