A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation
- 7 September 1990
- journal article
- case report
- Published by Elsevier BV in Cell
- Vol. 62 (5), 999-1006
- https://doi.org/10.1016/0092-8674(90)90274-i
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Type 1 fiber abnormalities in skeletal muscle of patients with hypertrophic and dilated cardiomyopathy: Evidence of subclinical myogenic myopathyJournal of the American College of Cardiology, 1989
- Sequence analysis of the complete Caenorhabditis elegans myosin heavy chain gene familyJournal of Molecular Biology, 1989
- Isolation and characterization of the complete human ?-myosin heavy chain geneHuman Genetics, 1989
- Relationship of the genes for Chediak-Higashi syndrome (beige) and the T-cell receptor γ chain in mouse and manGenomics, 1987
- Relationship between myosin isoenzyme composition, hemodynamics, and myocardial structure in various forms of human cardiac hypertrophy.Circulation Research, 1985
- MYOSINAnnual Review of Biochemistry, 1984
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1984
- A comprehensive set of sequence analysis programs for the VAXNucleic Acids Research, 1984
- Expression of recessive alleles by chromosomal mechanisms in retinoblastomaNature, 1983
- Familial Prevalence and Genetic Transmission of Idiopathic Hypertrophic Subaortic StenosisNew England Journal of Medicine, 1973