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Description
It functions as a redox-active peptide complex that interacts with copper-dependent enzymatic reactions

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Mitochondrial disease refers to a group of clinically heterogeneous disorders caused by dysfunction in the mitochondrial respiratory chain, often due to mutations in mitochondrial DNA (mtDNA) or nuclear DNA (nDNA) that encodes mitochondrial proteins

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[DOI] [PMC free article] [PubMed] [Google Scholar] [199].Sheldon AL, Robinson MB, The role of glutamate transporters in neurodegenerative diseases and potential opportunities for intervention, Neurochem

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