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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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| Publicado en: | Front Pharmacol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Frontiers Media S.A.
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6400831/ https://ncbi.nlm.nih.gov/pubmed/30873022 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2019.00121 |
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