Familial hypertrophic cardiomyopathy: diagnostic and therapeutic implications of recent genetic studies
Author:
Publisher
Elsevier BV
Subject
Genetics,Molecular Medicine
Reference43 articles.
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1. Mitochondrial Transcription Factors TFA, TFB1 and TFB2: A Search for DNA Variants/Haplotypes and the Risk of Cardiac Hypertrophy;Disease Markers;2008
2. Screening of the endothelin1 gene (EDN1) in a cohort of patients with essential left ventricular hypertrophy.;Annals of Human Genetics;2007-09
3. Side-to-side linking of myocardial cells in hypertrophic cardiomyopathy: Whole heart microscopic observation with tangential sections;Pathology International;2005-11
4. Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effect;International Journal of Cardiology;2005-07
5. Hypertrophic Cardiomyopathy: Low Frequency of Mutations in the β-Myosin Heavy Chain (MYH7) and Cardiac Troponin T (TNNT2) Genes among Spanish Patients;Clinical Chemistry;2003-08-01
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