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

Internet

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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