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Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system.
Janssen AJ, Schuelke M, Smeitink JA, Trijbels FJ, Sengers RC, Lucke B, Wintjes LT, Morava E, van Engelen BG, Smits BW, Hol FA, Siers MH, Ter Laak H, van der Knaap MS, Van Spronsen FJ, Rodenburg RJ, van den Heuvel LP. Janssen AJ, et al. Ann Neurol. 2008 Apr;63(4):473-81. doi: 10.1002/ana.21328. Ann Neurol. 2008. PMID: 18306232
Human diseases with defects in oxidative phosphorylation. 1. Decreased amounts of assembled oxidative phosphorylation complexes in mitochondrial encephalomyopathies.
Bentlage H, de Coo R, ter Laak H, Sengers R, Trijbels F, Ruitenbeek W, Schlote W, Pfeiffer K, Gencic S, von Jagow G, et al. Bentlage H, et al. Among authors: sengers r. Eur J Biochem. 1995 Feb 1;227(3):909-15. doi: 10.1111/j.1432-1033.1995.tb20218.x. Eur J Biochem. 1995. PMID: 7867654 Free article.
Human NADH:ubiquinone oxidoreductase.
Smeitink J, Sengers R, Trijbels F, van den Heuvel L. Smeitink J, et al. Among authors: sengers r. J Bioenerg Biomembr. 2001 Jun;33(3):259-66. doi: 10.1023/a:1010743321800. J Bioenerg Biomembr. 2001. PMID: 11695836
188 results