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Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm study. [electronic resource] by
- Rosenfeld, Margaret
- Wainwright, Claire E
- Higgins, Mark
- Wang, Linda T
- McKee, Charlotte
- Campbell, Daniel
- Tian, Simon
- Schneider, Jennifer
- Cunningham, Steve
- Davies, Jane C
Producer: 20190501
In:
The Lancet. Respiratory medicine vol. 6
Availability: No items available.
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