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Carnitine transporter mutations in Crohn's disease consists of missense mutation(s) in the gene coding plasma membrane transporter OCTN1 (SLC22A4) and/or mutation(s) in the promoter of the gene encoding OCTN2 (SLC22A5) [14, 35]
J Clin Pharmacol 43:12571267
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The developmental dismantling of pluripotency is reversed by ectopic Oct4 expression
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