| Literature DB >> 18938114 |
Teresa Collazo1, Ana María Bofill, Yulia Clark, Yadira Hernández, Manuel Gómez, Fidel Rodríguez, María D Ramos, Javier Giménez, Teresa Casals, Manuel Rojo.
Abstract
So far, more than 1500 mutations have been reported in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Mutational spectrum varies in accordance with geographic and/or ethnic origin. In this study, we have analyzed seven common CF mutations (p.F508del, p.G542X, p.R1162X, p.N1303K, p.R334W, p.R553X and c.3120+1G>A) taking into account the ethnic origin of the Cuban population which is mainly influenced by Spanish and sub-Sahara African contribution. All but p.N1303K have been detected in our patients, the p.F508del being the most prevalent (37.9%). Overall, six mutations showed frequencies above 1% accounting for 55.5% of the Cuban CF alleles.Entities:
Mesh:
Year: 2008 PMID: 18938114 DOI: 10.1016/j.jcf.2008.09.004
Source DB: PubMed Journal: J Cyst Fibros ISSN: 1569-1993 Impact factor: 5.482