GENETICS OF THE LONG QT SYNDROME

被引:12
作者
KEATING, M
机构
[1] UNIV UTAH, DIV CARDIOL, SALT LAKE CITY, UT 84112 USA
[2] UNIV UTAH, DEPT HUMAN GENET, SALT LAKE CITY, UT 84112 USA
关键词
LONG QT SYNDROME; CARDIAC ARRHYTHMIAS; LINKAGE ANALYSIS; MOLECULAR GENETICS; ION CHANNELS;
D O I
10.1111/j.1540-8167.1994.tb01155.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The application of molecular biology to human genetics has led to the development of a new field, human molecular genetics. This field has already had a dramatic impact on our understanding of cardiovascular disease and has helped improve diagnosis and treatment of these disorders. We have learned a great deal during the past decade about the long QT syndrome, familial hypertrophic cardiomyopathy, Duchenne muscular dystrophy, hypertension, and supravalvular aortic stenosis. In the coming decade, the pace of discovery will accelerate, offering new opportunities for the prediction and prevention of cardiovascular disease.
引用
收藏
页码:146 / 153
页数:8
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