Comparison of Mutation Profiles in the Duchenne Muscular Dystrophy Gene among Populations: Implications for Potential Molecular Therapies

Novel therapeutic approaches are emerging to restore dystrophin function in Duchenne Muscular Dystrophy (DMD), a severe neuromuscular disease characterized by progressive muscle wasting and weakness. Some of the molecular therapies, such as exon skipping, stop codon read-through and internal ribosom...

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Detalles Bibliográficos
Autores principales: López-Hernández, Luz Berenice, Gómez-Díaz, Benjamín, Luna-Angulo, Alexandra Berenice, Anaya-Segura, Mónica, Bunyan, David John, Zúñiga-Guzman, Carolina, Escobar-Cedillo, Rosa Elena, Roque-Ramírez, Bladimir, Ruano-Calderón, Luis Angel, Rangel-Villalobos, Héctor, López-Hernández, Julia Angélica, Estrada-Mena, Francisco Javier, García, Silvia, Coral-Vázquez, Ramón Mauricio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394478/
https://www.ncbi.nlm.nih.gov/pubmed/25761239
http://dx.doi.org/10.3390/ijms16035334

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