Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis

Glycogen storage disease type V (GSDV, McArdle disease) is a rare genetic myopathy caused by deficiency of the muscle isoform of glycogen phosphorylase (PYGM). This results in a block in the use of muscle glycogen as an energetic substrate, with subsequent exercise intolerance. The pathobiology of G...

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Detalles Bibliográficos
Autores principales: García-Consuegra, Inés, Asensio-Peña, Sara, Garrido-Moraga, Rocío, Pinós, Tomàs, Domínguez-González, Cristina, Santalla, Alfredo, Nogales-Gadea, Gisela, Serrano-Lorenzo, Pablo, Andreu, Antoni L., Arenas, Joaquín, Zugaza, José L., Lucia, Alejandro, Martín, Miguel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100117/
https://www.ncbi.nlm.nih.gov/pubmed/35563042
http://dx.doi.org/10.3390/ijms23094650

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100117/
https://www.ncbi.nlm.nih.gov/pubmed/35563042
http://dx.doi.org/10.3390/ijms23094650

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