“…Recently, a panel of 11 common mutations accounting overall for 70% of all Arab CF chromosomes have been reported : ΔF508del, 3120 + 1G " A, N1303K, W1282X, G115X, 711 + 1G " A, S549R, I1234V, 1548delG , H139L and 4010del4 [9]. The latter three mutations are believed to have originated in the Arab native populations since they were never described in Caucasian CF patients [5][6][7][8].…”