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 |
|---|---|
| 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 |
Research Groups and Themes
- Organic & Biological