Cystic fibrosis: A new mutation in the Lebanese population Chantal Farra, Rita Medawar, Salman Mroueh, Myrna Souaid, Faiza Cabet, Johnny Awwad  Journal of Cystic Fibrosis  Volume 7, Issue 5, Pages 429-432 (September 2008) DOI: 10.1016/j.jcf.2008.03.003 Copyright © 2008 European Cystic Fibrosis Society Terms and Conditions

Fig. 1 Sequence analysis of the 4016insG (exon 21) mutation in one of our homozygous patients (top) and in one of his heterozygous parents (middle). Wild-type sequence for comparison is shown in the bottom. In the homozygous individual, we can clearly see insertion of G followed by the T repeat. In the heterozygous individual, the 4016insG produces an overlap between the wild-type allele and the mutated allele. Journal of Cystic Fibrosis 2008 7, 429-432DOI: (10.1016/j.jcf.2008.03.003) Copyright © 2008 European Cystic Fibrosis Society Terms and Conditions