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Rescue of CFTR NBD2 mutants N1303K and S1235R is influenced by the functioning of the autophagosome
The missing phenylalanine at position 508, located in nucleotide-binding domain (NBD1) of the cystic fibrosis transmembrane regulator (CFTR), is the most common cystic fibrosis mutation. Severe disease-causing mutations also occur in NBD2. To provide information on potential therapeutic strategies f...
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| Publicado no: | J Cyst Fibros |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6435267/ https://ncbi.nlm.nih.gov/pubmed/29936070 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jcf.2018.05.016 |
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