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The treatment of cystic fibrosis has a long way to go as most of the existing therapeutics is for older children in addition to other limiting factors. Novel approaches like gene transfer/gene editing, disease modeling and search for alternative targets are warranted.

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This page is a summary of: Cystic fibrosis: current therapeutic targets and future approaches, Journal of Translational Medicine, April 2017, Springer Science + Business Media,
DOI: 10.1186/s12967-017-1193-9.
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