Defective pattern of mitochondrial respiratory enzymes in mitochondrial myopathy
- 1 September 1989
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 12 (3) , 373-377
- https://doi.org/10.1007/bf01799245
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- MTTOCHONDRIAL DNA DELETION IN ENCEPHALOMYOPATHYThe Lancet, 1988
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- Immunochemical study in three patients with cytochromec oxidase deficiency presenting leigh's encephalomyelopathyJournal of Inherited Metabolic Disease, 1987
- Two cases of NADH-coenzyme Q reductase deficiency: Relationship to MELAS syndromeThe Journal of Pediatrics, 1987
- Mitochondrial myopathiesAnnals of Neurology, 1985
- Two siblings with cytochromec oxidase deficiencyJournal of Inherited Metabolic Disease, 1983
- Mitochondria and diseaseMolecular Aspects of Medicine, 1980
- Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.Proceedings of the National Academy of Sciences, 1979
- Measurement of cytochromes in human skeletal muscle mitochondria, isolated from fresh and frozen stored muscle specimensBiochemical Medicine, 1978
- NONDROPLET ULTRASTRUCTURAL DEMONSTRATION OF CYTOCHROME OXIDASE ACTIVITY WITH A POLYMERIZING OSMIOPHILIC REAGENT, DIAMINOBENZIDINE (DAB)The Journal of cell biology, 1968