Developmental genetics of deleted mtDNA in mitochondrial oculomyopathy
- 1 February 1997
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 145 (2), 155-162
- https://doi.org/10.1016/s0022-510x(96)00241-9
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Normal variants of human mitochondrial DNA and translation products: the building of a reference data baseHuman Genetics, 1991
- Age-dependent increase in deleted mitochondrial DNA in the human heart: Possible contributory factor to presbycardiaAmerican Heart Journal, 1991
- Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathiesNucleic Acids Research, 1991
- Widespread multitissue deletions of the mitochondrial genome in the Pearson marrow-pancreas syndromeThe Journal of Pediatrics, 1990
- Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescenceBiochemical and Biophysical Research Communications, 1990
- Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNAAnnals of Neurology, 1989
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETIONThe Lancet, 1988
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- [49] Rapid DNA isolations for enzymatic and hybridization analysisMethods in Enzymology, 1980