Subdomain Location of Mutations in Cardiac Actin Correlate with Type of Functional Change
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference40 articles.
1. The genetic basis for cardiomyopathy: From mutation identification to mechanistic paradigms.;JG Seidman;Cell,2001
2. Identifying sarcomere gene mutations in hypertrophic cardiomyopathy: A personal history.;C Seidman;Circ Res,2011
3. Is there a common genetic basis for all familial cardiomyopathies?;A Perrot;Eur J Heart Fail,2007
4. Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy.;J Mogensen;J Clin Invest,1999
5. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure.;TM Olson;Science,1998
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