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CFTR structure and function: is there a role in the kidney?
Cystic fibrosis (CF) is a lethal autosomal recessive genetic disease caused by mutations in the CF transmembrane conductance regulator (CFTR). Mutations in the CFTR gene may result in a defective protein processing that leads to changes in function and regulation of this chloride channel. Despite of...
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| Udgivet i: | Biophys Rev |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Springer-Verlag
2009
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5387792/ https://ncbi.nlm.nih.gov/pubmed/28510151 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12551-008-0002-3 |
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