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duchenne muscular dystrophy and glutathione Mitochondrial creatine sensitivity is lost in the D2.mdx model of Duchenne muscular dystrophy and rescued by the mitochondrial-enhancing compound Olesoxime | American Journal of Physiology-Cell Physiology

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duchenne muscular dystrophy and glutathione Mitochondrial creatine sensitivity is lost in the D2.mdx model of Duchenne  muscular dystrophy and rescued by the mitochondrial-enhancing compound  Olesoxime | American Journal of Physiology-Cell Physiology
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