Article
[Clinical and molecular genetics of hypertrophic cardiomyopathy].
Orvosi hetilap - 16 Aug 1998
Sepp R, Csanády M
Abstract excerpt
Recent developments in molecular genetics have allowed to identify mutations in seven genes coding the beta myosin heavy chain, troponin T, alpha tropomyosin, myosin binding protein C, essential and regulatory myosin light chains and troponin I causing hypertrophic cardiomyopathy. These mutations...
Topics
- Cardiomyopathy, Hypertrophic
- Female
- Humans
- Male
- Molecular Biology
- Mutation
- World Health Organization
