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[DOI] [PubMed] [Google Scholar] [115].Hirsch HA, Iliopoulos D, Joshi A, Zhang Y, Jaeger SA, Bulyk M, et al

The CPT1A encoded protein is localized to the outer mitochondrial membrane where it exchanges carnitine onto long-chain fatty acyl-CoAs releasing the CoASH and generating a long-chain fatty acylcarnitine

Preterm neonates develop carnitine deficiency because of impaired proximal renal tubule carnitine reabsorption and immature carnitine biosynthesis