Distinct fibrosis pattern in desmosomal and phospholamban mutation carriers in hereditary cardiomyopathies-Reference-Cited by-同舟云学术

Distinct fibrosis pattern in desmosomal and phospholamban mutation carriers in hereditary cardiomyopathies

Published:2017-07 Issue:7 Volume:14 Page:1024-1032
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Sepehrkhouy Shahrzad,Gho Johannes M.I.H.,van Es René,Harakalova Magdalena,de Jonge Nicolaas,Dooijes Dennis,van der Smagt Jasper J.,Buijsrogge Marc P.,Hauer Richard N.W.,Goldschmeding Roel,de Weger Roel A.,Asselbergs Folkert W.,Vink Aryan

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference23 articles.

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3. Outcome in phospholamban R14del carriers: results of a large multicentre cohort study;van Rijsingen;Circ Cardiovasc Genet,2014

4. Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dyswplasia/cardiomyopathy genotype-phenotype follow-up study;Cox;Circulation,2011

5. Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: impact of genetics and revised task force criteria;Quarta;Circulation,2011

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