Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy
- 1 January 1992
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 107 (1) , 87-92
- https://doi.org/10.1016/0022-510x(92)90213-5
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Chronic progressive external ophthalmoplegia: A correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsiesJournal of the Neurological Sciences, 1990
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990
- Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNANucleic Acids Research, 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
- A Direct Repeat Is a Hotspot for Large-Scale Deletion of Human Mitochondrial DNAScience, 1989
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- Lumping or splitting? “ophthalmoplegia‐plus” or kearns‐sayre syndrome?Annals of Neurology, 1977
- NONDROPLET ULTRASTRUCTURAL DEMONSTRATION OF CYTOCHROME OXIDASE ACTIVITY WITH A POLYMERIZING OSMIOPHILIC REAGENT, DIAMINOBENZIDINE (DAB)The Journal of cell biology, 1968