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Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome

Mol Aspects Med (2013) 34(23):197219.10.1016/j.mam.2012.07.002 67 SeowHFBroerSBroerABaileyCGPotterSJCavanaughJAet alHartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19

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High OCTN1 levels in CD14 + monocytes/macrophages were also identified [112], while differentiation of monocytes into macrophages did not substantially change SLC22A4 expression [62, 93]