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Title: Human diseases with defects in oxidative phophorylation 1. Decreased amounts of assembled oxidative phosporylation complexes in mitochondrial encephalomyopathies
Author(s): Bentlage, H.A.C.M. ; Coo, I.F.M. de; Laak, H.J. ter ; Sengers, R.C.A. ; Trijbels, J.M.F. ; Ruitenbeek, W. ; Schlote, W.; Pfeiffer, K.; Gencic, S.; Jagow, G. von; Schägger, H.
Publication year: 1995
Source: European Journal of Biochemistry, vol. 227, (1995), pp. 909-915
ISSN: 0014-2956
DOI: https://doi.org/10.1111/j.1432-1033.1995.tb20218.x
Publication type: Article / Letter to editor

Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/188470   https://hdl.handle.net/2066/188470

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Subject: Characterization of the respiratory chain proteins in mitochondrial myopathies
Karakterisering van de eiwitten in de ademhalingsketen bij mitochondriële myopathieën
Organization: Paediatrics - OUD tm 2017
Human Genetics
Neurology
Journal title:
European Journal of Biochemistry
Volume: vol. 227
Page start: p. 909
Page end: p. 915

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