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Primary carnitine deficiency PCD is a rare genetic disease caused by mutations in the SLC22A5 gene, which leads to dysfunction of the carnitine transporter OCTN2, thereby hindering the entry of carnitine from the blood into cells and the reabsorption of carnitine by the kidneys

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Budui da se L-Carnitine Active+ preporua kao potpora procesu poticanja metabolizma masti i makronutrijenata u tijelu, primjeren je za aktivne odrasle osobe u dobi od 16 godina