Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC)-Reference-Cited by-同舟云学术

Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC)

Published:2018-05-21 Issue:7 Volume:29 Page:1004-1009
ISSN:1045-3873
Container-title:Journal of Cardiovascular Electrophysiology
language:en
Short-container-title:J Cardiovasc Electrophysiol

Author:

Murray Brittney¹,Hoorntje Edgar T.²³,te Riele Anneline S. J. M.³⁴,Tichnell Crystal¹,van der Heijden Jeroen F.⁴,Tandri Harikrishna¹,van den Berg Maarten P.⁵,Jongbloed Jan D. H.²,Wilde Arthur A. M.⁶,Hauer Richard N. W.³⁴,Calkins Hugh¹^ORCID,Judge Daniel P.¹,James Cynthia A.¹,van Tintelen J. Peter³⁷^ORCID,Dooijes Dennis⁸

Affiliation:

1. Division of Cardiology, Department of Medicine; Johns Hopkins University School of Medicine; Baltimore MD USA

2. Department of Genetics, University Medical Center Groningen; University of Groningen; Groningen the Netherlands

3. Netherlands Heart Institute; Utrecht the Netherlands

4. Division of Cardiology; University Medical Center Utrecht; Utrecht the Netherlands

5. Department of Cardiology, University of Groningen; University Medical Center Groningen; Groningen the Netherlands

6. Department of Cardiology, Academic Medical Centre, Heart Center; University of Amsterdam; Amsterdam The Netherlands

7. Department of Clinical Genetics, Amsterdam Cardiovascular Sciences; Academic Medical Center, University of Amsterdam; Amsterdam the Netherlands

8. Department of Medical Genetics; University Medical Center Utrecht; Utrecht the Netherlands

Funder

National Human Genome Research Institute

Netherlands Heart Foundation

Dutch Heart Foundation

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jce.13621/fullpdf

Reference19 articles.

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3. Clinical presentation, long-term follow-up, presentation, long-term follow-up, and outcomes of 1001 arrhythmogenic right ventricular dysplasia/cardiomyopathy patients and family members;Groeneweg;Circ Cardiovasc Genet,2015

4. Identification of Cadherin 2 (CDH2) mutations in arrhythmogenic right ventricular cardiomyopathy;Mayosi;Circ Cardiovasc Genet,2017

5. Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy;Hengel J;Eur Heart J,2013

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