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
收藏
页码：E163 / E163
页数：1
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