The Molecular Genetic Basis for Hypertrophic Cardiomyopathy
- 1 April 2001
- journal article
- review article
- Published by Elsevier BV in Journal of Molecular and Cellular Cardiology
- Vol. 33 (4), 655-670
- https://doi.org/10.1006/jmcc.2001.1340
Abstract
No abstract availableKeywords
This publication has 115 references indexed in Scilit:
- A transgenic rabbit model for human hypertrophic cardiomyopathyJCI Insight, 1999
- Structural Analysis of the Titin Gene in Hypertrophic Cardiomyopathy: Identification of a Novel Disease GeneBiochemical and Biophysical Research Communications, 1999
- Identification of a contractile deficit in adult cardiac myocytes expressing hypertrophic cardiomyopathy–associated mutant troponin T proteinsJCI Insight, 1999
- A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated β-myosin heavy chain genesHuman Genetics, 1998
- Effects of Two Hypertrophic Cardiomyopathy Mutations in α-Tropomyosin, Asp175Asn and Glu180Gly, on Ca2+Regulation of Thin Filament MotilityBiochemical and Biophysical Research Communications, 1997
- Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.JCI Insight, 1993
- Detection of a new mutation in the beta-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy.JCI Insight, 1992
- An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels.JCI Insight, 1990
- Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1New England Journal of Medicine, 1989
- Quantitative analysis of cardiac muscle cell disorganization in the ventricular septum of patients with hypertrophic cardiomyopathy.Circulation, 1979