Chronic progressive external ophthalmoplegia: A correlative study of quantitative molecular data and histochemical and biochemical profile
- 31 May 1994
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 123 (1-2) , 140-146
- https://doi.org/10.1016/0022-510x(94)90216-x
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNABiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1991
- Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial diseaseCell, 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
- Mitochondrial DNA mutations and neuromuscular diseaseTrends in Genetics, 1989
- Morphometric analyses of human muscle fiber typesMuscle & Nerve, 1982
- Sequence and organization of the human mitochondrial genomeNature, 1981
- Enzyme Activities in Skeletal Muscles from Patients with Peripheral Arterial InsufficiencyEuropean Journal of Clinical Investigation, 1976
- Metabolic Activity in Human Skeletal Muscle Effect of Peripheral Arterial InsufficiencyEuropean Journal of Clinical Investigation, 1972
- Expression of the mitochondrial genome in HeLa cellsJournal of Molecular Biology, 1971