Modulation of Ion Transport to Restore Airway Hydration in Cystic Fibrosis
Cystic fibrosis (CF) is a life-limiting genetic disorder caused by loss-of-function mutations in the gene which codes for the CF transmembrane conductance regulator (CFTR) Cl<sup>−</sup> channel. Loss of Cl<sup>−</sup> secretion across the apical membrane of airway lining epi...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2021-03-01
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| Series: | Genes |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2073-4425/12/3/453 |