A Mutation inTNNC1-encoded Cardiac Troponin C, TNNC1-A31S, Predisposes to Hypertrophic Cardiomyopathy and Ventricular Fibrillation
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Title
A Mutation inTNNC1-encoded Cardiac Troponin C, TNNC1-A31S, Predisposes to Hypertrophic Cardiomyopathy and Ventricular Fibrillation
Authors
Keywords
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Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 287, Issue 38, Pages 31845-31855
Publisher
American Society for Biochemistry & Molecular Biology (ASBMB)
Online
2012-07-20
DOI
10.1074/jbc.m112.377713
References
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Note: Only part of the references are listed.- Novel frameshift mutation in Troponin C ( TNNC1) associated with hypertrophic cardiomyopathy and sudden death
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- The cardiac troponin C mutation Leu29Gln found in a patient with hypertrophic cardiomyopathy does not alter contractile parameters in skinned murine myocardium
- (2009) Axel Neulen et al. BASIC RESEARCH IN CARDIOLOGY
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- Diagnostic, Prognostic, and Therapeutic Implications of Genetic Testing for Hypertrophic Cardiomyopathy
- (2009) J. Martijn Bos et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Functional Consequences of the Human Cardiac Troponin I Hypertrophic Cardiomyopathy Mutation R145G in Transgenic Mice
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- Challenging Current Paradigms Related to Cardiomyopathies
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- Modulation of troponin C affinity for the thin filament by different cross-bridge states in skinned skeletal muscle fibers
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- Familial hypertrophic cardiomyopathy-related cardiac troponin C mutation L29Q affects Ca2+ binding and myofilament contractility
- (2008) Bo Liang et al. PHYSIOLOGICAL GENOMICS
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