Functional Analysis of Myosin Mutations That Cause Familial Hypertrophic Cardiomyopathy-Reference-Cited by-同舟云学术

Functional Analysis of Myosin Mutations That Cause Familial Hypertrophic Cardiomyopathy

Published:1998-12 Issue:6 Volume:75 Page:3023-3030
ISSN:0006-3495
Container-title:Biophysical Journal
language:en
Short-container-title:Biophysical Journal

Author:

Roopnarine Osha,Leinwand Leslie A.

Publisher

Elsevier BV

Subject

Biophysics

Reference53 articles.

1. Point Mutations in Human β Cardiac Myosin Heavy Chain Have Differential Effects on Sarcomeric Structure and Assembly: An ATP Binding Site Change Disrupts Both Thick and Thin Filaments, Whereas Hypertrophic Cardiomyopathy Mutations Display Normal Assembly

2. A splice acceptor site mutation in the cardiac myosin binding protein C gene is associated with familial hypertrophic cardiomyopathy;Bonne;Nature Genet.,1995

3. Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy;Cuda;J. Clin. Invest.,1993

4. In vitro motility activity of β-cardiac myosin depends on the nature of the β-myosin heavy chain gene mutation in hypertrophic cardiomyopathy;Cuda;Circulation,1993

5. Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene;Dausse;J. Clin. Invest.,1993

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