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Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome

✍ Scribed by Yolanda Campos; Teresa Garcia-Silva; Carlos R. Barrionuevo; Ana Cabello; Rafael Muley; Joaquin Arenas

No coin nor oath required. For personal study only.

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