Functional Mitochondrial Heterogeneity in Heteroplasmic Cells Carrying the Mitochondrial DNA Mutation Associated with the MELAS Syndrome (Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes)
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J. Mazat | P. Frachon | A. Lombès | D. Sternberg | Annette C. Bakker | Cyrille Barthélémy | D. Château