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Description
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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When this enzyme is highly active, the body produces more eumelanin, which can lead to dark spots or an uneven skin tone
[DOI] [PMC free article] [PubMed] [Google Scholar] 117.Lavonas EJ, Akpunonu PD, Arens AM, et al
