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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]

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It is one of the most powerful antioxidants available and is both water and fat soluble

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AKI is a clinical condition hallmarked by a sudden decrease of renal function, whereas CKD is hallmarked by renal functional or structural impairments