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Description
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]
Kortam M, Abdelrahman R, Fateen H
Without sufficient carnitine, fatty acids cannot efficiently enter the mitochondria (even if there are abundant fat stores)
Hepatology 2004;40:652-659
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