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Exercise, Nutrition, and Supplements in the Muscle Carnitine Palmitoyl-Transferase II Deficiency: New Theoretical Bases for Potential Applications

Carnitine palmitoyltransferase II (CPTII) deficiency is the most frequent inherited disorder regarding muscle fatty acid metabolism, resulting in a reduced mitochondrial long-chain fatty acid oxidation during endurance exercise. This condition leads to a clinical syndrome characterized by muscle fat...

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Detalles Bibliográficos
Autores principales:	Negro, Massimo, Cerullo, Giuseppe, Parimbelli, Mauro, Ravazzani, Alberto, Feletti, Fausto, Berardinelli, Angela, Cena, Hellas, D’Antona, Giuseppe
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Physiology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365340/ https://www.ncbi.nlm.nih.gov/pubmed/34408664 http://dx.doi.org/10.3389/fphys.2021.704290

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