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The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability
The cystic fibrosis transmembrane conductance regulator (CFTR) is responsible for the disease cystic fibrosis (CF). It is a membrane protein belonging to the ABC transporter family functioning as a chloride/anion channel in epithelial cells around the body. There are over 1500 mutations that have be...
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| Publicat a: | Cell Mol Life Sci |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer International Publishing
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5209436/ https://ncbi.nlm.nih.gov/pubmed/27734094 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00018-016-2386-8 |
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