Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin Gene-Reference-Cited by-同舟云学术

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Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin Gene

Published:1997-03 Issue:3 Volume:29 Page:635-640
ISSN:0735-1097
Container-title:Journal of the American College of Cardiology
language:en
Short-container-title:Journal of the American College of Cardiology

Author:

Coviello Domenico A,Maron Barry J,Spirito Paolo,Watkins Hugh,Vosberg Hans-Peter,Thierfelder Ludwig,Schoen Frederick J,Seidman J.G,Seidman Christine E

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference20 articles.

1. α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy;Thierfelder;Cell,1994

2. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy;Watkins;Nature Genet,1995

3. Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy;Bonne;Nature Genet,1995

4. A molecular basis for familial hypertrophic cardiomyopathy;Geisterfer-Lowrence;Cell,1990

5. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy;Watkins;N Engl J Med,1992

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