Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers-Reference-Cited by-同舟云学术

Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers

Published:2013-04 Issue:4 Volume:15 Page:376-384
ISSN:1388-9842
Container-title:European Journal of Heart Failure
language:en
Short-container-title:European Journal of Heart Failure

Author:

van Rijsingen Ingrid A.W.¹,Nannenberg Eline A.²,Arbustini Eloisa³,Elliott Perry M.⁴,Mogensen Jens⁵,Hermans-van Ast Johanna F.⁶,van der Kooi Anneke J.⁷,van Tintelen J. Peter⁶⁸,van den Berg Maarten P.⁸,Grasso Maurizia³,Serio Alessandra³,Jenkins Sharon⁴,Rowland Camilla⁴,Richard Pascale⁹¹⁰,Wilde Arthur A.M.¹,Perrot Andreas¹¹,Pankuweit Sabine¹²,Zwinderman Aeilko H.¹³,Charron Philippe¹⁰,Christiaans Imke²,Pinto Yigal M.¹

Affiliation:

1. Department of Cardiology (Heart Failure Research Center); Academic Medical Center; Amsterdam The Netherlands

2. Department of Clinical Genetics; Academic Medical Center; Amsterdam The Netherlands

3. Department of Cardiology, Center for Heritable Cardiovascular Diseases; Fondazione IRCCS Policlinico San Matteo; Pavia Italy

4. Department of Cardiology; The Heart Hospital; London UK

5. Department of Cardiology; Aarhus University Hospital; Skejby Denmark

6. ICIN Netherlands Heart Institute/Durrer Center for Cardiogenetic Research; The Netherlands

7. Department of Neurology; Academic Medical Center; Amsterdam The Netherlands

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

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

10. Referral Center for Inherited Cardiac Diseases, UPMC Univ Paris 6, AP-HP, Hôpital Pitié-Salpêtrière; Paris France

11. Department of Cardiology, Experimental & Clinical Research Center; Charité-Universitaetsmedizin; Berlin Germany

12. Department of Cardiology; University Hospital Marburg; Germany

13. Department of Epidemiology; Academic Medical Center; Amsterdam The Netherlands

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Reference32 articles.

1. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B);Muchir;Hum Mol Genet,2000

2. Pushing the envelope on lipodystrophy;Flier;Nat Genet,2000

3. Lamin A/C and cardiac diseases;Sylvius;Curr Opin Cardiol,2006

4. Genotype-phenotype correlations in laminopathies: how does fate translate?;Scharner;Biochem Soc Trans,2010

5. The laminopathies: a clinical review;Rankin;Clin Genet,2006

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