Isabelle Fajac

Sep 25, 2024 | err.ersjournals.com | Isabelle Fajac

IntroductionCystic fibrosis (CF) is an autosomal recessive disorder caused by mutations in the CF transmembrane conductance regulator (CFTR) gene [1]. It is the most common life-shortening genetic disease in the Caucasian population, affecting at least 100 000 individuals worldwide [2]. The CFTR gene encodes the CFTR protein, which is a chloride and bicarbonate channel expressed at the cell membrane of many epithelial cells and other cell types, including inflammatory cells [3, 4].

Sep 9, 2023 | thelancet.com | Nicole Mayer-Hamblett |John Clancy |Scott Donaldson |Isabelle Fajac

These cookies are necessary for the website to function and cannot be switched off in our systems. They are usually only set in response to actions made by you which amount to a request for services, such as setting your privacy preferences, logging in or filling in forms. You can set your browser to block or alert you about these cookies, but some parts of the site will not then work. These cookies do not store any personally identifiable information.