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Novel mutation of the electron transferring flavoprotein dehydrogenase (ETFDH) gene in the isolated myopathic form of coenzyme q10 deficiency

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Q(10) deficiency, Mitochondrial encephalomyopathy, Science & technology, Life sciences & biomedicine, Biotechnology & applied microbiology, Genetics & heredity, Medical ethics, Medicine, research & experimental, Biotechnology & applied microbiology, Genetics & heredity, Medical ethics, Research & experimental medicine

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