Multiple Mutations in Genetic Cardiovascular Disease A Marker of Disease Severity?

被引：139

作者：

Kelly, Matthew ^{[1
,2
]}

Semsarian, Christopher ^{[1
,2
,3
]}

机构：

[1] Centenary Inst, Agnes Ginges Ctr Mol Cardiol, Sydney, NSW, Australia

[2] Univ Sydney, Fac Med, Sydney, NSW 2006, Australia

[3] Royal Prince Alfred Hosp, Dept Cardiol, Sydney, NSW, Australia

来源：

CIRCULATION-CARDIOVASCULAR GENETICS | 2009年 / 2卷 / 02期

基金：

英国医学研究理事会;

关键词：

cardiomyopathy; diagnosis; genetics; genetic heart disease; gene; cardiovascular; multiple mutation; disease severity; MYOSIN HEAVY-CHAIN; FAMILIAL HYPERTROPHIC CARDIOMYOPATHY; CARDIAC TROPONIN-T; LONG QT SYNDROME; MOUSE MODEL; DILATED CARDIOMYOPATHY; HEART-FAILURE; SUDDEN-DEATH; COMPOUND; PREVALENCE;

D O I：

10.1161/CIRCGENETICS.108.836478

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：182 / 190

页数：9

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