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Bomkamp, H

Carnitine palmitoyl transferase family Carnitine palmitoyltransferase 1A CPT1A is present mostly in the colon, duodenum, liver, kidney, and small intestine, and its deficiency results in a rare autosomal recessive metabolic disorder of long-chain FAO 19

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[DOI] [PMC free article] [PubMed] [Google Scholar] Banerjee Y, Pantea Stoian A, Cicero AFG, Fogacci F, Nikolic D, Sachinidis A, Rizvi AA, Janez A, Rizzo M, 2022

Primary carnitine deficiency (PCD) is a rare autosomal recessive disorder of fatty acid oxidation caused by deficiency of plasma membrane carnitine transport resulting from impairment in the plasma membrane OCTN2 carnitine transporter

doi: 10.1016/j.phymed.2022.154018, Summary Keywords chemical constituents, gut microbiota, hawthorn, lipid metabolism, medicinal and edible homologous plants Citation Xu H, Zhao X, Bai H and Li S (2026) Regulatory effects of hawthorn on lipid metabolic homeostasis: mechanisms, evidences, and perspectives