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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
This precaution ensures a thorough assessment of potential contraindications, contributing to the overall safety and efficacy of the procedure
[DOI] [PubMed] [Google Scholar] 4.Clarke G, et al
Saeed WK, Jun DW, Jang K, Oh JH, Chae YJ, Lee JS, et al
Suggested Usage: (Not intended to be used as a concentrate)
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