Artículo
CFTR gene analysis in Latin American CF patients: heterogeneous origin and distribution of mutations across the continent
Registro en:
1569-1993
10.1016/j.jcf.2006.07.004
Autor
Pérez, Martín M.
Luna, María Cecilia
Pivetta, Omar H.
Keyeux, Genoveva
Resumen
Fil: Pérez, Martín M. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina. Fil: Luna, María Cecilia. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina. Fil: Pivetta, Omar H. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina. Fil: Keyeux, Genoveva. Universidad Nacional de Colombia. Instituto de Genética; Bogotá, Colombia. Cystic Fibrosis (CF) is the most prevalent Mendelian disorder in European populations. Despite the fact that many Latin American countries have a predominant population of European-descent, CF has remained an unknown entity until recently. Argentina and Brazil have detected the first patients around three decades ago, but in most countries this disease has remained poorly documented. Recently, other countries started publishing their results.