Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans

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Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans Empty Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans

Post  Jon Moulton on Mon Nov 09, 2015 11:50 am

Shamseldin HE, Smith LL, Kentab A, Alkhalidi H, Summers B, Alsedairy H, Xiong Y, Gupta VA, Alkuraya FS. Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans. Hum Genet. 2015 Nov 5. [Epub ahead of print]
Jon Moulton
Jon Moulton

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