Arrhythmogenic right ventricular dysplasia/cardiomyopathy: Pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study

Circulation

Volumn 123, Issue 23, 2011, Pages 2690-2700

  Cox, Moniek G P J ^a,i   Van Der Zwaag, Paul A ^b   Van Der Werf, Christian ^c   Van Der Smagt, Jasper J ^a   Noorman, Maartje ^a,i   Bhuiyan, Zahir A ^c   Wiesfeld, Ans C P ^b   Volders, Paul G A ^d   Van Langen, Irene M ^b   Atsma, Douwe E ^e   Dooijes, Dennis ^a   Van Den Wijngaard, Arthur ^d   Houweling, Arjan C ^f   Jongbloed, Jan D H ^b   Jordaens, Luc ^g   Cramer, Maarten J ^a   Doevendans, Pieter A ^a   De Bakker, Jacques M T ^a,c,i   Wilde, Arthur A M ^c,i   Van Tintelen, J Peter ^b,h   Hauer, Richard N W ^a,i   more..

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^c ACADEMIC MEDICAL CENTER   (Netherlands)

^d MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^e LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^f VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^g ERASMUS MEDICAL CENTER   (Netherlands)

^h Durrer Center for Cardiogenetic Research   (Netherlands)

ⁱ ROYAL NETHERLANDS ACADEMY OF ARTS AND SCIENCES   (Netherlands)

Author keywords

arrhythmogenic right ventricular dysplasia; cardiomyopathy; desmosome; follow up studies; genetics

Indexed keywords

DESMOCOLLIN; DESMOGLEIN 2; DESMOPLAKIN; PLAKOGLOBIN; PLAKOPHILIN;

ADULT; ARTICLE; CARDIOVASCULAR RISK; CONTROLLED STUDY; DESMOSOME; DNA DETERMINATION; EXON; FAMILY ASSESSMENT; FEMALE; FOLLOW UP; GENE DELETION; GENE MUTATION; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HEART RIGHT VENTRICLE DYSPLASIA; HUMAN; MAJOR CLINICAL STUDY; MALE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; PRIORITY JOURNAL; SAINT MARTIN (DUTCH);

ADOLESCENT; ADULT; ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA; ASYMPTOMATIC DISEASES; DEATH, SUDDEN, CARDIAC; DESMOSOMES; FAMILY; FEMALE; FOLLOW-UP STUDIES; GENOTYPE; HUMANS; MALE; MIDDLE AGED; NETHERLANDS; PHENOTYPE; PREDICTIVE VALUE OF TESTS; RISK FACTORS; TACHYCARDIA, VENTRICULAR; VENTRICULAR FIBRILLATION; YOUNG ADULT;

EID: 79959568500     PISSN: 00097322     EISSN: 15244539     Source Type: Journal    
DOI: 10.1161/CIRCULATIONAHA.110.988287     Document Type: Article

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