Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment?

BACKGROUND: McArdle disease is caused by myophosphorylase deficiency and results in complete inability for muscle glycogen breakdown. A hallmark of this condition is muscle oxidation impairment (e.g., low peak oxygen uptake (VO(2peak))), a phenomenon traditionally attributed to reduced glycolytic fl...

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Detalles Bibliográficos
Autores principales: Villarreal-Salazar, M., Santalla, A., Real-Martínez, A., Nogales-Gadea, G., Valenzuela, P.L., Fiuza-Luces, C., Andreu, A.L., Rodríguez-Aguilera, J.C., Martín, M.A., Arenas, J., Vissing, J., Lucia, A., Krag, T.O., Pinós, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9758572/
https://www.ncbi.nlm.nih.gov/pubmed/36455789
http://dx.doi.org/10.1016/j.molmet.2022.101648

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9758572/
https://www.ncbi.nlm.nih.gov/pubmed/36455789
http://dx.doi.org/10.1016/j.molmet.2022.101648

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