Functional Consequences of a Mutation in an Expressed Human α-Cardiac Actin at a Site Implicated in Familial Hypertrophic Cardiomyopathy
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference32 articles.
1. The Genetic Basis for Cardiomyopathy
2. α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
3. Clinical and genetic characteristics of cardiac actin gene mutations in hypertrophic cardiomyopathy
4. Inherited and de novo Mutations in the Cardiac Actin Gene Cause Hypertrophic Cardiomyopathy
5. Prevalence and Spectrum of Thin Filament Mutations in an Outpatient Referral Population With Hypertrophic Cardiomyopathy
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