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Description
Metabolism and disposition of intravenously administered acetyl-L-carnitine in healthy volunteers Eur J Clin Pharmacol 1989
Currently, there is no genetic cure for Systemic Primary Carnitine Deficiency (SPCD), which is also sometimes called OCTN2 deficiency or Carnitine Transporter Deficiency [1] [2] [3]
J.GivskovM.FiorentiniC.KrejsgaardT
The specific factors causing this malodour are unclear, and there are no targeted treatment options to counteract it effectively
