Arrhythmogenic Right Ventricular Cardiomyopathy Toward a Modern Clinical and Genomic Understanding

被引：6

作者：

Dunn, Kyla E. ^{[1
,2
,3
]}

Ashley, Euan A. ^{[1
,2
]}

机构：

[1] Stanford Univ, Sch Med, Ctr Inherited Cardiovasc Dis, Dept Med, Stanford, CA 94305 USA

[2] Stanford Univ, Sch Med, Ctr Inherited Cardiovasc Dis, Dept Genet, Stanford, CA 94305 USA

[3] Stanford Childrens Hlth, Lucile Packard Childrens Hosp, Pediat Heart Ctr, Palo Alto, CA USA

来源：

CIRCULATION-CARDIOVASCULAR GENETICS | 2015年 / 8卷 / 03期

关键词：

Editorials; arrhythmogenic right ventricular cardiomyopathy; arrhythmogenic right ventricular dysplasia; arrhythmogenic right ventricular dysplasia-cardiomyopathy; TASK-FORCE CRITERIA; HYPERTROPHIC CARDIOMYOPATHY; PHYSICAL-ACTIVITY; BRUGADA SYNDROME; FAMILY-MEMBERS; MUTATIONS; DIAGNOSIS; DYSPLASIA/CARDIOMYOPATHY; PHENOTYPE; RISK;

D O I：

10.1161/CIRCGENETICS.115.001119

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：421 / 424

页数：4

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