l-carnitine source Naturals Capsules 250mg, 120 ct L-Carnitine Liquid, Citrus Flavor 1000
Description
demonstrated that memory loss in old rats is associated with brain mitochondrial decay and RNA/DNA oxidation
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
An intriguing history is related to another member of the OCTN family, namely OCTN3 (SLC22A21)
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To view a copy of this licence, visit About this article Cite this article Pesta, M., Mrazova, B., Kapalla, M
