Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS)
- 1 September 1989
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 92 (2-3) , 143-158
- https://doi.org/10.1016/0022-510x(89)90132-9
Abstract
No abstract availableThis publication has 41 references indexed in Scilit:
- Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyBiochemical and Biophysical Research Communications, 1988
- Deficiency of subunits of complex I or IV in mitochondrial myopathies: Immunochemical and immunohistochemical studyJournal of Inherited Metabolic Disease, 1987
- INTRACELLULAR CALCIUM HOMEOSTASISAnnual Review of Biochemistry, 1987
- Benign Mitochondrial Myopathy with Deficiency of NADH-CoQ Reductase and Cytochrome c OxidaseNeuropediatrics, 1986
- Deficiency of subunits in heart mitochondrial NADH-ubiquinone oxidoreductase of a patient with mitochondrial encephalomyopathy and cardiomyopathyBiochemical and Biophysical Research Communications, 1986
- Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke‐like episodes syndrome and NADH‐CoQ reductase deficiencyJournal of Inherited Metabolic Disease, 1986
- MITOCHONDRIAL ENCEPHALOMYOPATHIESBrain, 1982
- Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy.Archives of Disease in Childhood, 1981
- Cloning of human mitochondrial DNA in Escherichia coliJournal of Molecular Biology, 1980
- Studies on the electron transfer system IV. The electron transfer particleBiochimica et Biophysica Acta, 1956