Učitavanje...
Genetic therapies for cystic fibrosis lung disease
The aim of gene therapy for cystic fibrosis (CF) lung disease is to efficiently and safely express the CF transmembrane conductance regulator (CFTR) in the appropriate pulmonary cell types. Although CF patients experience multi-organ disease, the chronic bacterial lung infections and associated infl...
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| Glavni autori: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Oxford University Press
2011
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3095059/ https://ncbi.nlm.nih.gov/pubmed/21422098 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr104 |
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