Abstract
In cystic fibrosis, ion-transport abnormalities cause problems in many organs. A small molecule that forms cell-membrane pores which allow ion transport, shows promise in studies of human cells and an animal model of the disease. See Letter p. 405.
Original language | English |
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Pages (from-to) | 315-317 |
Number of pages | 3 |
Journal | Nature |
Volume | 567 |
Issue number | 7748 |
Early online date | 13 Mar 2019 |
DOIs | |
Publication status | Published - 21 Mar 2019 |