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Biochimica Et Biophysica Acta|December 2, 2008
Isolated deficiencies of OXPHOS complexes I and IV are identified accurately and quickly by simple enzyme activity immunocapture assaysJ H Willis, R A Capaldi, M Huigsloot, et al.
Biochimica Et Biophysica Acta|November 25, 1993
Tissue distribution of cytochrome c oxidase isoforms in mammals. Characterization with monoclonal and polyclonal antibodiesJ W Taanman, R E Hall, C Tang, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
A novel mtDNA mutation in the ATPase6 gene studied by E. coli modelingR Carrozzo, J Murray, O Capuano, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1984
31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscleS Eleff, N G Kennaway, N R Buist, et al.
The Journal of Biological Chemistry|December 22, 2000
Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patternsR H Triepels, B J Hanson, L P van den Heuvel, et al.
Pediatric Research|November 1, 1990
Isoforms of mammalian cytochrome c oxidase: correlation with human cytochrome c oxidase deficiencyN G Kennaway, R D Carrero-Valenzuela, G Ewart, et al.
American Journal of Human Genetics|September 16, 1999
A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathyS Rahman, J W Taanman, J M Cooper, et al.
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