Long-Range Effects of Familial Hypertrophic Cardiomyopathy Mutations E180G and D175N on the Properties of Tropomyosin
Author:
Affiliation:
1. Cardiovascular Program, Boston Biomedical Research Institute, 64 Grove Street, Watertown, Massachusetts 02472, United States
2. Neurology Department, Harvard Medical School, Boston, Massachusetts 02114, United States
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi3006835
Reference57 articles.
1. Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy
2. Sarcomeric Proteins and Familial Hypertrophic Cardiomyopathy: Linking Mutations in Structural Proteins to Complex Cardiovascular Phenotypes
3. Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy
4. α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
5. Novel missense mutation in α-tropomyosin gene found in Japanese patients with hypertrophic cardiomyopathy
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