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Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency
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(2020) 6:e000928
[PubMed] [Google Scholar] 27.Lee GC, Tam CP, Danesh-Meyer HV, Myers JS, Katz LJ
Finally, we investigated whether the functional mitochondrial defects in ccOzz / and, to a lesser extent, Alix / myotubes were associated with histochemical changes in the muscle tissue, as typically observed in human mitochondrial myopathies 10,12
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