Cystic fibrosis (CF) is the most common lethal genetic disorder, caused by mutations in the gene encoding for Cystic Fibrosis Transmembrane Conductance Regulator (CFTR), a channel responsible for chloride (Cl−) and bicarbonate (HCO3−) transport in epithelial cells [1,2]. This evidence concerns the gene CFTR and cystic fibrosis.