DNA Analysis in Inherited Cardiomyopathies: Current Status and Clinical Relevance
Author:
Publisher
Wiley
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1540-8159.2008.00956.x/fullpdf
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2. The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands;Alders;Eur Heart J,2003
3. Can electrocardiographic changes help to identify the causative mutation in hereditary hypertrophic cardiomyopathy?;Arens;Suppl Circul,2005
4. The genetic bases of cardiomyopathies;Richard;J Am Coll Cardiol,2006
5. Prevalence and severity of “benign” mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy;Van Driest;Circulation,2002
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