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Publikováno v:
BMJ Case Reports. 15:e251321
The neonatal form of carnitine palmitoyltransferase II (CPT II) deficiency is a rare lethal inherited disorder of fatty acid oxidation. Carnitine essentially transfers long-chain fatty acids across the mitochondrial membranes for β-oxidation, where
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d68536345187d40ae8a6e3ff081142a
https://doi.org/10.1136/bcr-2022-251321
https://doi.org/10.1136/bcr-2022-251321
