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
Jon Moulton 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- Posts : 5721
Join date : 2010-03-12
Age : 61
Location : Philomath, Oregon, USA -
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