Robust method for TALEN-edited correction of pF508del in patient-specific induced pluripotent stem cells

Cystic fibrosis is one of the most frequent inherited rare diseases, caused by mutations in the cystic fibrosis transmembrane conductance regulator gene. Apart from symptomatic treatments, therapeutic protocols for curing the disease have not yet been established. The regeneration of genetically cor...

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Detalles Bibliográficos
Autores principales: Camarasa, María Vicenta, Gálvez, Víctor Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748475/
https://www.ncbi.nlm.nih.gov/pubmed/26861665
http://dx.doi.org/10.1186/s13287-016-0275-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748475/
https://www.ncbi.nlm.nih.gov/pubmed/26861665
http://dx.doi.org/10.1186/s13287-016-0275-6

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