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Frataxin activates mitochondrial energy conversion and oxidative phosphorylation

Friedreich's ataxia (FA) is an autosomal recessive disease caused by decreased expression of the mitochondrial protein frataxin. The biological function of frataxin is unclear. The homologue of frataxin in yeast, YFH1, is required for cellular respiration and was suggested to regulate mitochond...

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מידע ביבליוגרפי
Main Authors: Ristow, Michael, Pfister, Markus F., Yee, Andrew J., Schubert, Markus, Michael, Laura, Zhang, Chen-Yu, Ueki, Kojhiro, Michael, M. Dodson, Lowell, Bradford B., Kahn, C. Ronald
פורמט: Artigo
שפה:Inglês
יצא לאור: The National Academy of Sciences 2000
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC17325/
https://ncbi.nlm.nih.gov/pubmed/11035806
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