Deficiency of Subunits of Complex I or IV in Mitochondrial Myopathies: Immunochemical and Immunohistochemical Study

Overview

Journal J Inherit Metab Dis

Publisher Wiley

Date 1987 Jan 1

PMID 2828762

Citations 6

Authors

M Tanaka

M Nishikimi

H Suzuki

M Tada

T Ozawa

Y Koga

I Nonaka

Affiliations

Soon will be listed here.

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NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findings.

Pitkanen S, Feigenbaum A, Laframboise R, Robinson B J Inherit Metab Dis. 1996; 19(5):675-86.

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Muscle pathology in cytochrome c oxidase deficiency.

Nonaka I, Koga Y, Shikura K, Kobayashi M, Sugiyama N, Okino E Acta Neuropathol. 1988; 77(2):152-60.

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Cytochrome c oxidase deficiency in infancy.

Oldfors A, Sommerland H, Holme E, Tulinius M, Kristiansson B Acta Neuropathol. 1989; 77(3):267-75.

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Congenital deficiency of a 20-kDa subunit of mitochondrial complex I in fibroblasts.

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References

Tanaka M, Nishikimi M, Suzuki H, Ozawa T, Koga Y, Nonaka I . Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies. Biochem Int. 1987; 14(3):525-30. View

Tanaka M, Nishikimi M, Suzuki H, Ozawa T, Ichiki T, Kobayashi M . Variation in the levels of complex I subunits among tissues in a patient with mitochondrial encephalomyopathy and renal dysfunction. Biochem Int. 1987; 14(4):735-9. View

Chomyn A, Cleeter M, Ragan C, Riley M, Doolittle R, Attardi G . URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit. Science. 1986; 234(4776):614-8. DOI: 10.1126/science.3764430. View

Tanaka M, Nishikimi M, Suzuki H, Ozawa T, Nishizawa M, Tanaka K . Deficiency of subunits in heart mitochondrial NADH-ubiquinone oxidoreductase of a patient with mitochondrial encephalomyopathy and cardiomyopathy. Biochem Biophys Res Commun. 1986; 140(1):88-93. DOI: 10.1016/0006-291x(86)91061-2. View

Capaldi R . Arrangement of proteins in the mitochondrial inner membrane. Biochim Biophys Acta. 1982; 694(3):291-306. DOI: 10.1016/0304-4157(82)90009-0. View