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Description
Clin Biochem
[6] Stephens, F
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]
For this reason, many take carnitine as a weight loss supplement to help bump up fat burning
