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Xu H, et al

Changes in NCV and amplitude were also assessed at baseline and follow-up as a neurophysiological measure of DPN

Genetic deficiencies of transporter activity represent the only known forms of primary carnitine deficiency [27]
Carnitine is found almost exclusively (99%) intracellularly, existing either as free LC or as several species of acyl-carnitine esters, predominantly in the muscle and liver
