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Restoration of W1282X CFTR Activity by Enhanced Expression
Cystic fibrosis results from mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Premature termination codons represent a common minority of CFTR mutations, and are caused by base pair substitutions that produce abnormal stop codons in the coding sequence. Select aminog...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Thoracic Society
2007
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1994229/ https://ncbi.nlm.nih.gov/pubmed/17541014 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1165/rcmb.2006-0176OC |
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