Topical cystic fibrosis transmembrane conductance regulator gene replacement for cystic fibrosis‐related lung disease
Background Cystic fibrosis is caused by a defective gene encoding a protein called the cystic fibrosis transmembrane conductance regulator (CFTR), and is characterised by chronic lung infection resulting in inflammation and progressive lung damage that results in a reduced life expectancy. Objective...
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Veröffentlicht in: | Cochrane database of systematic reviews 2016-06, Vol.2016 (7), p.CD005599-CD005599 |
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