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Matsuishi T, Hirata K, Terasawa K et al : Successful carnitine treatment in two siblings having lipid storage myopathy with hypertrophic cardiomyopathy

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Our developers chose L-carnitine L-tartrate because it has been shown to enter the bloodstream faster and has a higher bioavailability, making it particularly effective

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