Complements of the house.
editorial · Level V
Where this comes from
- Record sourced from PubMed, PMID 15372098.
- Also identified by PMC identifier 516272.
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Abstract
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.
Medical subject headings
- Electron Transport Complex I