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[Abstract] Chin J Nat Med

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Beauty extends beyond the skin

10.1017/S0954422412000054 54 TothP

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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