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Higgins, C

Clinical Significance: Acyl Carnitine Translocase Deficiency Mutations in the SLC25A20 gene , which encodes Acyl Carnitine Translocase , lead to Carnitine-Acylcarnitine Translocase Deficiency (CACT Deficiency)

doi: 10.1016/j.jff.2016.12.038

47 ShangF.ZhangJ.LiZ.ZhangJ.YinY.WangY.et al (2016)

If you experience any new, persistent, or concerning symptoms whilst taking Mounjaro, contact your healthcare provider promptly for assessment and guidance