Ascertainment strategies and genotype: Phenotype correlations in hypertrophic cardiomyopathy

被引:3
作者
Blair, E [1 ]
Redwood, C [1 ]
Watkins, H [1 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Dept Cardiovasc Med, Oxford OX3 9DU, England
关键词
D O I
10.1161/01.CIR.0000081440.49766.A6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:E24 / E24
页数:1
相关论文
共 4 条
[1]   Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy [J].
Blair, E ;
Price, SJ ;
Baty, CJ ;
Östman-Smith, I ;
Watkins, H .
JOURNAL OF MEDICAL GENETICS, 2001, 38 (06) :385-387
[2]  
Richard P, 2001, CIRCULATION, V104, P521
[3]   The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms [J].
Seidman, JG ;
Seidman, C .
CELL, 2001, 104 (04) :557-567
[4]   Prevalence and severity of "Benign" mutations in the β-myosin heavy chain, cardiac troponin T, and α-tropomyosin genes in hypertrophic cardiomyopathy [J].
Van Driest, SL ;
Ackerman, MJ ;
Ommen, SR ;
Shakur, R ;
Will, ML ;
Nishimura, RA ;
Tajik, AJ ;
Gersh, BJ .
CIRCULATION, 2002, 106 (24) :3085-3090