Syntaxin 8 and the Endoplasmic Reticulum Processing of ΔF508-CFTR
Background/Aims: Cystic fibrosis (CF) is a lethal recessive disorder caused by mutations in the CF transmembrane conductance regulator (CFTR). ΔF508, the most common mutation, is a misfolded protein that is retained in the endoplasmic reticulum and degraded, precluding delivery to the cell surface [...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cell Physiol Biochem Press GmbH & Co KG
2018-11-01
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| coleção: | Cellular Physiology and Biochemistry |
| Assuntos: | |
| Acesso em linha: | https://www.karger.com/Article/FullText/495596 |
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