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Description
CPT1 (CPT1A) deficiency is an extremely rare, autosomal recessively inherited disorder, with only some 60 cases worldwide reported so far
B., Sitta, A., Deon, M., Wajner, M., and Vargas, C

Additionally, L-Carnitine acts as a transporter for removing toxic compounds from the mitochondria, preventing their buildup in these cellular organelles

Biomed Pharmacother= Biomed Pharmacother 143, 112139
