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Furthermore, cellular metabolism is inherently complex, and the fate of accumulated lactate can be influenced by multiple variables, potentially diverting it away from Kla

Park Y, Lee HJ, Sim DY, et al

D., Triantafyllou, K

Genetic CPT1A deficiency is a very rare occurrence, but patients generally present with hypoketotic hypoglycemia and hepatic encephalopathy due to defects in long-chain FAO (27)

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