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Introduction Primary carnitine deficiency (PCD, OMIM #212140) is an autosomal recessive disorder of fatty acid beta-oxidation caused by a dysfunctional OCTN2 carnitine transporter, coded by the SLC22A5 gene on chromosome five (Shoji et al
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Importance of Glyteine As the immediate precursor to glutathione, Glyteine is the only nutrient with proven clinical bioavailability to take glutathione well beyond homeostasis within hours of taking a single dose [11]
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