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Luke E. Formosa et al.
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Assembly factors for the membrane arm of human complex I
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Evidence that the assembly of the yeast cytochrome bc(1) complex involves the formation of a large core structure in the inner mitochondrial membrane
Vincenzo Zara et al.
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SE Ong et al.
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Blue Native electrophoresis to study mitochondrial and other protein complexes
LGJ Nijtmans et al.
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V Tiranti et al.
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Supercomplexes in the respiratory chains of yeast and mammalian mitochondria
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