Unequal abundance of mutated myosin among individual cardiomyocytes: the trigger for myocardial phenotype development in familial hypertrophic cardiomyopathy related to beta-myosin mutations?

被引：0
|
作者：
Kraft, T. [1 ]
Montag, J. [1 ]
Tripathi, S. [1 ]
Dunda, S. [1 ]
Syring, M. [1 ]
Nedel, S. [1 ]
Perrot, A. [2 ]
Francino, A. [3 ]
Navarro-Lopez, F. [3 ]
Brenner, B. [3 ]
机构：
[1] Hannover Med Sch, Hannover, Germany
[2] Charite Campus Berlin Buch CBB, Berlin, Germany
[3] Hosp Clin Barcelona, Barcelona, Spain
来源：
EUROPEAN HEART JOURNAL | 2014年 / 35卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P6147
引用
收藏
页码：1085 / 1085
页数：1
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