Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference21 articles.
1. Prevalence of hypertrophic cardiomyopathy in a general population of young adults: echocardiographic analysis of 4,111 subjects in the CARDIA study: Coronary Artery Risk Development in (Young) Adults;Maron;Circulation,1995
2. The FHC Mutation Database, ANGIS 2001. Available at: http://morgan.angis.su.oz.au/Databases/Heart/dbsearch.html. Accessed April 22, 2004.
3. Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy;Erdmann;Clin Genet,2003
4. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy;Richard;Circulation,2003
5. Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden;Morner;J Mol Cell Cardiol,2003
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