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Published byRalf Damian Bradley Modified over 6 years ago
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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 (September 2008) DOI: /j.jcf Copyright © 2008 European Cystic Fibrosis Society Terms and Conditions
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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, DOI: ( /j.jcf ) Copyright © 2008 European Cystic Fibrosis Society Terms and Conditions
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