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In many cases, optimising nutritional status and addressing the underlying cause is as important as the isolated blood carnitine concentration

SLC22A5 mutations impair OCTN2 function, causing primary carnitine deficiency (PCD) ( Beyond genetic determinants, OCTN2 expression and function undergo significant physiological and pharmacological regulation

[DOI] [PubMed] [Google Scholar] 132.Glenn J.M., Gray M., Wethington L.N., Stone M.S., Stewart R.W., Jr., Moyen N.E

Its structure allows it to neutralize oxidative damage, reduce the aging process, and enhance physical and mental performance