Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy

We assessed the potential of Lmna-mRNA repair by spliceosome-mediated RNA trans-splicing as a therapeutic approach for LMNA-related congenital muscular dystrophy. This gene therapy strategy leads to reduction of mutated transcript expression for the benefit of corresponding wild-type (WT) transcript...

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Detalles Bibliográficos
Autores principales: Azibani, Feriel, Brull, Astrid, Arandel, Ludovic, Beuvin, Maud, Nelson, Isabelle, Jollet, Arnaud, Ziat, Esma, Prudhon, Bernard, Benkhelifa-Ziyyat, Sofia, Bitoun, Marc, Lorain, Stéphanie, Bonne, Gisèle, Bertrand, Anne T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862133/
https://www.ncbi.nlm.nih.gov/pubmed/29499949
http://dx.doi.org/10.1016/j.omtn.2017.12.012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862133/
https://www.ncbi.nlm.nih.gov/pubmed/29499949
http://dx.doi.org/10.1016/j.omtn.2017.12.012

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