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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

Elevated plasma lipopolysaccharide (LPS) during edematous episodes has been implicated as a trigger for cytokine production and immune activation [164]

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[PMC free article] [PubMed] [Google Scholar] 72.Vanella A, Russo A, Acquaviva R, Campisi A, Di Giacomo C, Sorrenti V, Barcellona ML

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