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Mutation-specific dual potentiators maximize rescue of CFTR gating mutants
BACKGROUND: The potentiator ivacaftor (VX-770) has been approved for therapy of 38 cystic fibrosis (CF) mutations (~10% of the patient population) associated with a gating defect of the CF transmembrane conductance regulator (CFTR). Despite the success of VX-770 treatment of patients carrying at lea...
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| Veröffentlicht in: | J Cyst Fibros |
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| Hauptverfasser: | , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7190413/ https://ncbi.nlm.nih.gov/pubmed/31678009 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jcf.2019.10.011 |
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