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How should L-carnitine be taken orally

Klarich, K

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mutations in OCTN2 lead to primary carnitine deficiency (PCD), a disorder characterized by systemic carnitine depletion and associated clinical manifestations, including muscle weakness, cardiomyopathy, and infertility

Application of the transduction protocol for drug discovery using an antibody designed against -synuclein In order to test the transduction protocol, we used it to administer a rationally designed anti-aggregation single-domain antibody, called DesAb-F 35 , to a PD worm model (Fig

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