MiRNAs, Myostatin, and Muscle MRI Imaging as Biomarkers of Clinical Features in Becker Muscular Dystrophy

Becker muscular dystrophy (BMD) is an X-linked recessive disorder caused by dystrophin gene mutations. The phenotype and evolution of this muscle disorder are extremely clinical variable. In the last years, circulating biomarkers have acquired remarkable importance in their use as noninvasive biolog...

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Detalles Bibliográficos
Autores principales: Marozzo, Roberta, Pegoraro, Valentina, Angelini, Corrado
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554733/
https://www.ncbi.nlm.nih.gov/pubmed/32961888
http://dx.doi.org/10.3390/diagnostics10090713

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554733/
https://www.ncbi.nlm.nih.gov/pubmed/32961888
http://dx.doi.org/10.3390/diagnostics10090713

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