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Die Forschung zeigt, dass Carnitin die Konzentration des Neurotransmitters erhht und seine Funktion auf mitochondrialer Ebene optimiert
Adv Cancer Res (2017) 136:10938
Apr 2021;37(4):332-336
Mutations in the major carnitine transporter, encoded by the SLC22A5 gene [also known as zwitterion/cation transporter 2 (OCTN2)], are the predominant causes of primary carnitine deficiency
Nephrolithiasis: molecular mechanism of renal stone formation and the critical role played by modulators
