Cardiac troponin T mutation, Arg92Trp, linked to familial hypertrophic cardiomyopathy shows a high disease penetrance, moderate hypertrophy, and early progression to dilated cardiomyopathy-like features in Japanese

被引:0
|
作者
Shimizu, M [1 ]
Ino, H [1 ]
Okeie, K [1 ]
Emoto, Y [1 ]
Yamaguchi, M [1 ]
Yasuda, T [1 ]
Fujii, H [1 ]
Fujita, S [1 ]
Mabuchi, H [1 ]
机构
[1] Kanazawa Univ, Kanazawa, Ishikawa 920, Japan
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中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
4311
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页码:817 / 817
页数:1
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  • [2] Autopsy findings in siblings with hypertrophic cardiomyopathy caused by Arg92Trp mutation in the cardiac troponin T gene showing dilated cardiomyopathy-like features
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