17-Year Follow-up Study of a Patient With Obstructive Hypertrophic Cardiomyopathy With a Deletion Mutation in the Cardiac Myosin Binding Protein C Gene
Author:
Affiliation:
1. The Second Department of Internal Medicine, Ehime University School of Medicine
2. Department of Geriatric Medicine, Ehime University School of Medicine
3. Medical Research Institute, Tokyo Medical and Dental University
Publisher
Japanese Circulation Society
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
http://www.jstage.jst.go.jp/article/circj/68/2/68_2_174/_pdf
Reference18 articles.
1. Structural Analysis of the Titin Gene in Hypertrophic Cardiomyopathy: Identification of a Novel Disease Gene
2. Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.
3. Mutations in the Genes for Cardiac Troponin T and α-Tropomyosin in Hypertrophic Cardiomyopathy
4. Mutations in the Gene for Cardiac Myosin-Binding Protein C and Late-Onset Familial Hypertrophic Cardiomyopathy
5. Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein.
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1. Phenotypic Characterization of a Family With An In-frame Deletion in the DMD Gene and Variable Penetrance;Current Gene Therapy;2018-10-04
2. Pharmacogenetic Interactions Between Angiotensin-Converting Enzyme Insertion/Deletion Polymorphism and Response to Cibenzoline in Patients With Hypertrophic Obstructive Cardiomyopathy;Journal of Cardiovascular Pharmacology;2010-05
3. A985G Polymorphism of the Endothelin-2 Gene and Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy;Circulation Journal;2007
4. A Japanese Patient With Cardiomyopathy Caused by a Novel Mutation R285X in the AGL Gene;Circulation Journal;2007
5. Morphologic Characteristics of Hypertrophic Cardiomyopathy of the Elderly With Cardiac Myosin-Binding Protein C Gene Mutations;Circulation Journal;2006
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