
Finding mutations in nuclear genes responsible for disorders in the mitochondrial oxidative phosphorylation system has been a tedious matter. A "Venn diagram" approach--not unlike a classic complementation experiment--reported in this issue will now make the search easier.
Electron Transport Complex I, Models, Genetic, Humans, Models, Biological, Oxidative Phosphorylation, Mitochondria
Electron Transport Complex I, Models, Genetic, Humans, Models, Biological, Oxidative Phosphorylation, Mitochondria
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