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V.SequeiraJ
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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Clinical trial data and post-marketing surveillance indicate that a subset of patients experience decreased energy, tiredness, and general malaise while taking these medications
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What are the risks of compounded GLP-1 medications
doi:10.1111/j.1600-0560.1991.tb01542.x
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