Eric A. Schon
J Clin Invest.
2004;
114(6):760–762
doi:10.1172/JCI22942
This article Copyright © 2004, The American Society for Clinical Investigation
Abstract
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Full text
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F
inding 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.
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