SLC26A9 and cystic fibrosis: Absence of basal Cl− secretion in airways of CF patients carrying the type II mutation F508del-CFTR (De Boeck and Amaral, 2016), is probably due to the lack of expression of SLC26A9 in the apical membrane (Figure 2B) (El Khouri and Toure, 2014; Bertrand et al., 2017).