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MicroRNAs as serum biomarkers in Becker muscular dystrophy

Becker muscular dystrophy (BMD) is an X‐linked neuromuscular disorder due to mutation in the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is characterized by progressive muscle degeneration and proximal muscle weakness. Interestingly, a dysregulated expression of muscle‐sp...

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Detalles Bibliográficos
Autores principales:	Gagliardi, Delia, Rizzuti, Mafalda, Brusa, Roberta, Ripolone, Michela, Zanotti, Simona, Minuti, Elisa, Parente, Valeria, Dioni, Laura, Cazzaniga, Sara, Bettica, Paolo, Bresolin, Nereo, Comi, Giacomo Pietro, Corti, Stefania, Magri, Francesca, Velardo, Daniele
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443944/ https://www.ncbi.nlm.nih.gov/pubmed/35880500 http://dx.doi.org/10.1111/jcmm.17462

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