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Phenotyping of Rare CFTR Mutations Reveals Distinct Trafficking and Functional Defects
Background. The most common CFTR mutation, F508del, presents with multiple cellular defects. However, the possible multiple defects caused by many rarer CFTR mutations are not well studied. We investigated four rare CFTR mutations E60K, G85E, E92K and A455E against well-characterized mutations, F508...
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| Publicado no: | Cells |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7140603/ https://ncbi.nlm.nih.gov/pubmed/32204475 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells9030754 |
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