Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy-Reference-Cited by-同舟云学术

Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy

Published:2016-11-03 Issue:4 Volume:19 Page:512-521
ISSN:1388-9842
Container-title:European Journal of Heart Failure
language:en
Short-container-title:Eur J Heart Fail

Author:

Jansweijer Joeri A.¹,Nieuwhof Karin²,Russo Francesco³,Hoorntje Edgar T.²,Jongbloed Jan D.H.²,Lekanne Deprez Ronald H.³,Postma Alex V.⁴,Bronk Marieke³,van Rijsingen Ingrid A.W.¹,de Haij Simone³,Biagini Elena⁵,van Haelst Paul L.⁶,van Wijngaarden Jan⁷,van den Berg Maarten P.⁸,Wilde Arthur A.M.¹,Mannens Marcel M.A.M.³,de Boer Rudolf A.⁸,van Spaendonck-Zwarts Karin Y.³,van Tintelen J. Peter²³,Pinto Yigal M.¹

Affiliation:

1. AMC Heart Center, Department of Clinical and Experimental Cardiology, Academic Medical Center Amsterdam; University of Amsterdam; Amsterdam The Netherlands

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

3. Department of Clinical Genetics, Academic Medical Center Amsterdam; University of Amsterdam; Amsterdam The Netherlands

4. Department of Anatomy, Embryology and Physiology, Academic Medical Center Amsterdam; University of Amsterdam; Amsterdam The Netherlands

5. Department of Cardiology; S. Orsola-Malpighi Hospital; Bologna University Italy

6. Department of Cardiology; Antonius Hospital; Sneek The Netherlands

7. Department of Cardiology; Deventer Hospital; Deventer The Netherlands

8. Department of Cardiology, University Medical Center Groningen; University of Groningen; Groningen The Netherlands

Funder

Netherlands CardioVascular Research Initiative: the Dutch Heart Foundation

Dutch Federation of University Medical Centres

Netherlands Organisation for Health Research and Development

the Royal Netherlands Academy of Sciences

ARENA

PREDICT

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejhf.673/fullpdf

Reference31 articles.

1. Dilated cardiomyopathy: the complexity of a diverse genetic architecture;Hershberger;Nat Rev Cardiol,2013

2. Genetic testing for dilated cardiomyopathy in clinical practice;Lakdawala;J Card Fail,2012

3. Truncations of titin causing dilated cardiomyopathy;Herman;N Engl J Med,2012

4. Exome sequencing and genome-wide linkage analysis in 17 families illustrates the complex contribution of TTN truncating variants to dilated cardiomyopathy;Norton;Circ Cardiovasc Genet,2013

5. Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy;Spaendonck-Zwarts;Eur Heart J,2014

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