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Autor:
Prins, Stella, Langron, Emily, Hastings, Cato, Hill, Emily J., Stefan, Andra C., Griffin, Lewis D., Vergani, Paola *
Publikováno v:
In Journal of Biological Chemistry 4 December 2020 295(49):16529-16544
Autor:
Prins, Stella, Langron, Emily, Hastings, Cato, Hill, Emily J., Stefan, Andra C., Griffin, Lewis D., Vergani, Paola
Cystic fibrosis (CF) is a life-limiting disease caused by mutations in the human CFTR gene, encoding an anion-selective channel. Because CF-causing mutations affect both CFTR permeation/gating and biogenesis, multi-assay approaches have been implemen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=sharebioRxiv::af346c7e7bb25bdfdb269d0822fd1314
