l-carnitine mitochondrial disease Disorders of long-chain fatty acid oxidation and the carnitine shuttle | Reviews in Endocrine and Metabolic Disorders L-Carnitine in Drosophila: A Review
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Furthermore, significant alterations in the carnitine/acylcarnitine pathway were detected in bladder cancer patients
doi: 10.1111/ceo.14218 569 LiMZhangLPanLZhouPYuRZhangZet al
Similar content being viewed by others Introduction Propionic acidemia (PA) is an inborn error metabolic disorder caused by mutations in the gene responsible for encoding propionyl-CoA carboxylase (PCC)
