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mutations in OCTN2 lead to primary carnitine deficiency (PCD), a disorder characterized by systemic carnitine depletion and associated clinical manifestations, including muscle weakness, cardiomyopathy, and infertility

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doi: 10.2337/db05-1145 Summary Keywords GLP-1RA, tumor diseases, function, mechanism, agonists Citation Ji L, He X, Min X, Yang H, Wu W, Xu H, Chen J and Mei A (2024) Glucagon-like peptide-1 receptor agonists in neoplastic diseases

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PMID 3031680