Hypertrophic cardiomyopathy: single gene disease or complex trait?
Author:
Publisher
Oxford University Press (OUP)
Subject
Cardiology and Cardiovascular Medicine
Link
http://academic.oup.com/eurheartj/article-pdf/37/23/1823/6733595/ehv562.pdf
Reference17 articles.
1. Mutations in cardiac myosin heavy chain genes cause familial hypertrophic cardiomyopathy;Seidman;Mol Biol Med,1991
2. Mutation Type Is Not Clinically Useful in Predicting Prognosis in Hypertrophic Cardiomyopathy
3. Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers;Claes;Eur Heart J,2016
4. Double or compound sarcomere mutations in hypertrophic cardiomyopathy: A potential link to sudden death in the absence of conventional risk factors
5. Cardiac Structural and Sarcomere Genes Associated With Cardiomyopathy Exhibit Marked Intolerance of Genetic Variation
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