Cystic Fibrosis (CF) is a lethal autosomal recessive disease where mutation ΔF508 (loss of phenylalanine residue at position 508) in the gene encoding Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) is responsible for the abnormal mucus secretions (Rowe et al., 2005). Here, CFTR is linked to cystic fibrosis.