The impact of 12 months treatment with ivacaftor on Scottish paediatric patients with cystic fibrosis with the G551D mutation: a review | Archives of Disease in Childhood

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The impact of 12 months treatment with ivacaftor on Scottish paediatric patients with cystic fibrosis with the G551D mutation: a review

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Cite this article as:: Dryden C, Wilkinson J, Young D on behalf of the Scottish Paediatric Cystic Fibrosis Managed Clinical Network (SPCFMCN), et al

The impact of 12 months treatment with ivacaftor on Scottish paediatric patients with cystic fibrosis with the G551D mutation: a review

Archives of Disease in Childhood 2018;103:68-70.