CellWell record HH-0464
Copper supplementation restores cytochrome c oxidase assembly defect in a mitochondrial disease model of COA6 deficiency
Ghosh A, Trivedi PP, Timbalia SA, Griffin AT, Rahn JJ, Chan SSL, Gohil VM
Human Molecular Genetics ยท 2014
In plain language
In a cellular model, copper supplementation restored assembly of cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain, illustrating copper's essential cofactor role in cellular energy production.
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Cite this record: https://thecellwell.org/studies/HH-0464
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