Exome Sequencing of Atrioventricular Septal Defects Reveals Rare and de novo Variants in Genes Related to Congenital Heart Disease and Cardiac Development

被引：0

作者：

Priest, James R. ^{[1
]}

Girirajan, Santhosh ^{[2
]}

Dewey, Frederick ^{[1
]}

Eichler, Evan E. ^{[3
]}

Gelb, Bruce D. ^{[4
]}

Quertermous, Tom ^{[1
]}

Ashley, Euan A. ^{[1
]}

Portman, Michael A. ^{[3
]}

机构：

[1] Stanford Univ, Med Ctr, Stanford, CA 94305 USA

[2] Penn State Univ, College Stn, PA USA

[3] Univ Washington, Seattle, WA 98195 USA

[4] Icahn Sch Med Mt Sinai, New York, NY USA

来源：

CIRCULATION RESEARCH | 2013年 / 113卷 / 12期

关键词：

Atrioventricular canal; Genetics; Congenital heart disease; Gene mutations; Pediatric cardiology;

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：E163 / E163

页数：1

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