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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

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Current research has shown that mild cognitive impairment in Parkinsons patients is associated with brain energy metabolism (23)