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Mitochondrial stress responses in Duchenne muscular dystrophy: metabolic dysfunction or adaptive reprogramming? American Journal of Physiology Cell Physiology American Physiological Society Duchenne breakthrough therapy leaves behind pioneering families 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 American Physiological Society Characteristics of Duchenne muscular dystrophy (DMD). (A) Typically, Download Scientific Diagram
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