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mtDNA T8993G mutation-induced F1F0-ATP synthase defect augments mitochondrial dysfunction associated with hypoxia/reoxygenation: the protective role of melatonin.
Wen-Yi Huang, Mei-Jie Jou, Tsung-I Peng
PLoS ONE · 2013
doi:10.1371/journal.pone.0081546
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