A mutation in the beta-myosin rod associated with hypertrophic cardiomyopathy has an unexpected molecular phenotype
Journal Article
Overview
publication date
- January 1, 2010
has subject area
- Adenosine Triphosphatases - Ventricular Myosins
- Amino Acids, Acidic - Glutamic Acid
- Amino Acids, Basic - Lysine
- Amino Acids, Diamino - Lysine
- Amino Acids, Dicarboxylic - Glutamic Acid
- Amino Acids, Essential - Lysine
- Aortic Valve Disease - Cardiomyopathy, Hypertrophic
- Cardiomyopathies - Cardiomyopathy, Hypertrophic
- Cytoskeletal Proteins - Ventricular Myosins
- Excitatory Amino Acids - Glutamic Acid
- Humans
- Macromolecular Substances - Ventricular Myosins
- Muscle Proteins - Ventricular Myosins
- Mutagenesis - Amino Acid Substitution
- Mutation
- Phenotype
- Protein Engineering - Amino Acid Substitution
- Protein Stability
- Protein Structure, Secondary
- Thermodynamics
has restriction
- green
Date in CU Experts
- September 6, 2013 4:09 AM
Full Author List
- Armel TZ; Leinwand LA
author count
- 2
citation count
- 10
published in
Other Profiles
International Standard Serial Number (ISSN)
- 0006-291X
Electronic International Standard Serial Number (EISSN)
- 1090-2104
Digital Object Identifier (DOI)
Additional Document Info
start page
- 352
end page
- 356
volume
- 391
issue
- 1