Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy
Published 2020 View Full Article
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Title
Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy
Authors
Keywords
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Journal
HEART
Volume -, Issue -, Pages heartjnl-2020-316913
Publisher
BMJ
Online
2020-05-26
DOI
10.1136/heartjnl-2020-316913
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Related references
Note: Only part of the references are listed.- Clinical Course and Management of Hypertrophic Cardiomyopathy
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- (2015) Montse Olivé et al. HUMAN MOLECULAR GENETICS
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- The role of ubiquitin ligases in cardiac disease
- (2013) Monte S. Willis et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Human Molecular Genetic and Functional Studies Identify TRIM63 , Encoding Muscle RING Finger Protein 1, as a Novel Gene for Human Hypertrophic Cardiomyopathy
- (2012) Suet Nee Chen et al. CIRCULATION RESEARCH
- Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases
- (2012) C. Rapezzi et al. EUROPEAN HEART JOURNAL
- Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms
- (2009) Giulia Mearini et al. CARDIOVASCULAR RESEARCH
- 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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