标题
Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy
作者
关键词
-
出版物
HEART
Volume -, Issue -, Pages heartjnl-2020-316913
出版商
BMJ
发表日期
2020-05-26
DOI
10.1136/heartjnl-2020-316913
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Clinical Course and Management of Hypertrophic Cardiomyopathy
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- New cardiac and skeletal protein aggregate myopathy associated with combined MuRF1 and MuRF3 mutations
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- In This Issue
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- 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy
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- Rare Variants in Genes Encoding MuRF1 and MuRF2 Are Modifiers of Hypertrophic Cardiomyopathy
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- Human Molecular Genetic and Functional Studies Identify TRIM63 , Encoding Muscle RING Finger Protein 1, as a Novel Gene for Human Hypertrophic Cardiomyopathy
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- Build it up-Tear it down: protein quality control in the cardiac sarcomere
- (2008) M. S. Willis et al. CARDIOVASCULAR RESEARCH
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