No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy-Reference-Cited by-同舟云学术

No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy

Published:2018-08-30 Issue:8 Volume:13 Page:e0203078
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Hoorntje Edgar T.^ORCID,Posafalvi Anna,Syrris Petros^ORCID,van der Velde K. Joeri^ORCID,Bolling Marieke C.,Protonotarios Alexandros^ORCID,Boven Ludolf G.,Amat-Codina Nuria,Groeneweg Judith A.,Wilde Arthur A.,Sobreira Nara,Calkins Hugh,Hauer Richard N. W.,Jonkman Marcel F.,McKenna William J.,Elliott Perry M.^ORCID,Sinke Richard J.^ORCID,van den Berg Maarten P.,Chelko Stephen P.,James Cynthia A.,van Tintelen J. Peter,Judge Daniel P.,Jongbloed Jan D. H.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference37 articles.

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4. Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members;JA Groeneweg;Circ Cardiovasc Genet,2015

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1. Combining whole exome sequencing with in silico analysis and clinical data to identify candidate variants in pediatric left ventricular noncompaction;International Journal of Cardiology;2022-01

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