Emerging Therapeutic Approaches for Cystic Fibrosis. From Gene Editing to Personalized Medicine

An improved understanding of the cystic fibrosis (CF) transmembrane conductance regulator (CFTR) protein structure and the consequences of CFTR gene mutations have allowed the development of novel therapies targeting specific defects underlying CF. Some strategies are mutation specific and have alre...

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Detalles Bibliográficos
Autores principales: Pranke, Iwona, Golec, Anita, Hinzpeter, Alexandre, Edelman, Aleksander, Sermet-Gaudelus, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400831/
https://www.ncbi.nlm.nih.gov/pubmed/30873022
http://dx.doi.org/10.3389/fphar.2019.00121

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400831/
https://www.ncbi.nlm.nih.gov/pubmed/30873022
http://dx.doi.org/10.3389/fphar.2019.00121

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