HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

被引：352

作者：

Ackerman, Michael J. ^{[1
]}

Priori, Silvia G. ^{[2
,3
]}

Willems, Stephan ^{[4
]}

Berul, Charles ^{[5
,6
]}

Brugada, Ramon ^{[7
,8
]}

Calkins, Hugh ^{[9
]}

Camm, A. John ^{[10
]}

Ellinor, Patrick T. ^{[11
]}

Gollob, Michael ^{[12
]}

Hamilton, Robert ^{[13
]}

Hershberger, Ray E. ^{[14
]}

Judge, Daniel P. ^{[9
,15
]}

Le Marec, Herve ^{[16
]}

McKenna, William J. ^{[17
]}

Schulze-Bahr, Eric ^{[18
]}

Semsarian, Chris ^{[19
]}

Towbin, Jeffrey A. ^{[20
]}

Watkins, Hugh ^{[21
]}

Wilde, Arthur ^{[22
]}

Wolpert, Christian ^{[23
]}

Zipes, Douglas P. ^{[24
]}

机构：

[1] Mayo Clin, Rochester, MN USA

[2] Univ Pavia, Fdn Salvatore Maugeri, I-27100 Pavia, Italy

[3] NYU, New York, NY USA

[4] Univ Hosp Hamburg Eppendorf, Hamburg, Germany

[5] Childrens Natl Med Ctr, Washington, DC USA

[6] George Washington Sch Med, Washington, DC USA

[7] Girona Inst Biomed Res, Girona, Spain

[8] Univ Girona, Sch Med, Girona, Spain

[9] Johns Hopkins Univ, Baltimore, MD USA

[10] St Georges Univ London, London, England

[11] Massachusetts Gen Hosp, Cardiac Arrhythmia Serv, Boston, MA 02114 USA

[12] Univ Ottawa, Inst Heart, Ottawa, ON, Canada

[13] Hosp Sick Children, Toronto, ON, Canada

[14] Univ Miami, Miller Sch Med, Miami, FL 33136 USA

[15] Univ Paris 05, Paris, France

[16] Inst Thorax, Nantes, France

[17] UCL, Inst Cardiovasc Sci, London, England

[18] Univ Hosp Muenster, Munster, Germany

[19] Univ Sydney, Sydney, NSW 2006, Australia

[20] Cincinnati Childrens Hosp, Cincinnati, OH USA

[21] Univ Oxford, John Radcliffe Hosp, Oxford OX3 9DU, England

[22] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands

[23] Ludwigsburg Clin, Ludwigsburg, Germany

[24] Indiana Univ, Sch Med, Krannert Inst Cardiol, Indianapolis, IN 46202 USA

来源：

EUROPACE | 2011年 / 13卷 / 08期

关键词：

Genetics; Cardiomyopathies; Channelopathies; LONG-QT SYNDROME; RIGHT-VENTRICULAR CARDIOMYOPATHY; SUDDEN CARDIAC DEATH; OF-FUNCTION MUTATION; IMPLANTABLE CARDIOVERTER-DEFIBRILLATOR; GENOTYPE-PHENOTYPE CORRELATION; FAMILIAL DILATED CARDIOMYOPATHY; RYANODINE RECEPTOR GENE; ST-SEGMENT ELEVATION; HYPERTROPHIC CARDIOMYOPATHY;

D O I：

10.1093/europace/eur245

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：1077 / 1109

页数：33

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