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Description
Cederbaum SD, Koo-McCoy S, Tein I, Hsu BY, Ganguly A, Vilain E, Dipple K, Cvitanovic-Sojat L, Stanley C: Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency
Greater use of glucose by the glycolytic pathway has also been reported in mice in which mitochondrial -oxidation is impaired ( Reference Wicks, Vandanmagsar and Haynie 62 , Reference Tavecchio, Lisanti and Bennett 76 )
PMID: 36821461
Methods Enzymol 1986
Med Sci Sports Exerc 14(5):377381
Do not skip that because you are in a hurry
