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135 (1): 21-30 (2016)
Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans.
HE Shamseldin
,
LL Smith
,
A Kentab
Notes
[Original String]:
12. Shamseldin HE, Smith LL, Kentab A, et al. Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans. Human genetics 2016;135(1):21-30 doi: 10.1007/s00439-015-1608-8[published Online First: Epub Date]