Distinct Fiber Type Signature in Mouse Muscles Expressing a Mutant Lamin A Responsible for Congenital Muscular Dystrophy in a Patient

Specific mutations in LMNA, which encodes nuclear intermediate filament proteins lamins A/C, affect skeletal muscle tissues. Early-onset LMNA myopathies reveal different alterations of muscle fibers, including fiber type disproportion or prominent dystrophic and/or inflammatory changes. Recently, we...

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Detalles Bibliográficos
Autores principales: Barateau, Alice, Vadrot, Nathalie, Agbulut, Onnik, Vicart, Patrick, Batonnet-Pichon, Sabrina, Buendia, Brigitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492014/
https://www.ncbi.nlm.nih.gov/pubmed/28441765
http://dx.doi.org/10.3390/cells6020010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492014/
https://www.ncbi.nlm.nih.gov/pubmed/28441765
http://dx.doi.org/10.3390/cells6020010

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