Characterization of mitochondrial DNA in primary cardiomyopathies
- 1 December 1995
- journal article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 243 (2) , 181-189
- https://doi.org/10.1016/0009-8981(95)06166-5
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- An efficient method for PCR analysis of mitochondrial DNA from paraffin-embedded archival heart tissue.Genome Research, 1995
- Concepts of autoimmunity applied to idiopathic dilated cardiomyopathyJournal of the American College of Cardiology, 1993
- Angiotensin-converting enzyme DD genotype in patients with ischaemic or idiopathic dilated cardiomyopathyThe Lancet, 1993
- Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11Nature Genetics, 1993
- Molecular Genetic Aspects of CardiomyopathyBiochemical Medicine and Metabolic Biology, 1993
- A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3Nature Genetics, 1993
- Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart diseaseMutation Research/DNAging, 1992
- Age-dependent increase in deleted mitochondrial DNA in the human heart: Possible contributory factor to presbycardiaAmerican Heart Journal, 1991
- Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1New England Journal of Medicine, 1989
- Sequence and organization of the human mitochondrial genomeNature, 1981