COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency | Journal of Medical Genetics

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Mitochondrial genetics

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COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency

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Cite this article as:: Martinez Lyons A, Ardissone A, Reyes A, et al

COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency

Journal of Medical Genetics 2016;53:846-849.