Overexpression of CUGBP1 in Skeletal Muscle from Adult Classic Myotonic Dystrophy Type 1 but Not from Myotonic Dystrophy Type 2

Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are progressive multisystemic disorders caused by similar mutations at two different genetic loci. The common key feature of DM pathogenesis is nuclear accumulation of mutant RNA which causes aberrant alternative splicing of specific pre-mRNAs by alte...

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Detalles Bibliográficos
Autores principales: Cardani, Rosanna, Bugiardini, Enrico, Renna, Laura V., Rossi, Giulia, Colombo, Graziano, Valaperta, Rea, Novelli, Giuseppe, Botta, Annalisa, Meola, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869793/
https://www.ncbi.nlm.nih.gov/pubmed/24376746
http://dx.doi.org/10.1371/journal.pone.0083777

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869793/
https://www.ncbi.nlm.nih.gov/pubmed/24376746
http://dx.doi.org/10.1371/journal.pone.0083777

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