Multicenter Study of the Prevalence and Distribution of Sarcometric Gene Mutations in Familial Hypertrophic Cardiomyopathy
Author:
Affiliation:
1. Department of Cardio-Angiology, Kitasato University School of Medicine
Publisher
Japanese Circulation Society
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
http://www.jstage.jst.go.jp/article/circj/76/2/76_CJ-11-1260/_pdf
Reference12 articles.
1. Contemporary Definitions and Classification of the Cardiomyopathies
2. A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation
3. Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond
4. 4. Frank D, Kuhn C, Katus HA, Frey N. The sarcomeric Z-disc: A nodal point in signalling and disease. J Mol Med 2006; 84: 446-468.
5. Hypertrophic Cardiomyopathy
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2. Mutation Analysis of the Main Hypertrophic Cardiomyopathy Genes Using Multiplex Amplification and Semiconductor Next-Generation Sequencing;Circulation Journal;2014
3. Biochemical and Physiological Regulation of Cardiac Myocyte Contraction by Cardiac-Specific Myosin Light Chain Kinase;Circulation Journal;2013
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