Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: Results of a systematic screening-Reference-Cited by-同舟云学术

Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: Results of a systematic screening

Published:2014-11 Issue:11 Volume:11 Page:1999-2009
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Roux-Buisson Nathalie,Gandjbakhch Estelle,Donal Erwan,Probst Vincent,Deharo Jean-Claude,Chevalier Philippe,Klug Didier,Mansencal Nicolas,Delacretaz Etienne,Cosnay Pierre,Scanu Patrice,Extramiana Fabrice,Keller Dagmar,Hidden-Lucet Françoise,Trapani Jonathan,Fouret Pierre,Frank Robert,Fressart Veronique,Fauré Julien,Lunardi Joel,Charron Philippe

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference33 articles.

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3. Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy;Gerull;Nat Genet,2004

4. Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy;Pilichou;Circulation,2006

5. DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy;Awad;Am J Hum Genet,2006

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