Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy
- 1 December 2004
- journal article
- Published by Elsevier in Journal of the American College of Cardiology
- Vol. 44 (12) , 2315-2325
- https://doi.org/10.1016/j.jacc.2004.05.088
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathyNature Genetics, 1997
- Diagnostic Value of Electrocardiography and Echocardiography for Familial Hypertrophic Cardiomyopathy in a Genotyped Adult PopulationCirculation, 1997
- Hypertrophic cardiomyopathyThe Lancet, 1997
- Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families.Heart, 1997
- Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscleNature Genetics, 1996
- Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathyNature Genetics, 1995
- Mutations in the cardiac myosin binding protein–C gene on chromosome 11 cause familial hypertrophic cardiomyopathyNature Genetics, 1995
- Prevalence of Hypertrophic Cardiomyopathy in a General Population of Young AdultsCirculation, 1995
- α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomereCell, 1994
- A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutationPublished by Elsevier ,1990