CFTR gene analysis in Latin American CF patients: heterogeneous origin and distribution of mutations across the continent

dc.creatorPérez, Martín M.
dc.creatorLuna, María Cecilia
dc.creatorPivetta, Omar H.
dc.creatorKeyeux, Genoveva
dc.date2021-01-20T12:51:03Z
dc.date2021-01-20T12:51:03Z
dc.date2007-05
dc.date.accessioned2023-08-29T20:09:01Z
dc.date.available2023-08-29T20:09:01Z
dc.identifier1569-1993
dc.identifierhttps://www.cysticfibrosisjournal.com/action/showPdf?pii=S1569-1993%2806%2900119-6
dc.identifierhttp://sgc.anlis.gob.ar/handle/123456789/2178
dc.identifier10.1016/j.jcf.2006.07.004
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8520459
dc.descriptionFil: Pérez, Martín M. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.
dc.descriptionFil: Luna, María Cecilia. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.
dc.descriptionFil: Pivetta, Omar H. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.
dc.descriptionFil: Keyeux, Genoveva. Universidad Nacional de Colombia. Instituto de Genética; Bogotá, Colombia.
dc.descriptionCystic 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.
dc.languageen
dc.relationJournal of cystic fibrosis
dc.rightsnone
dc.subjectFibrosis Quística
dc.subjectRegulador de Conductancia de Transmembrana de Fibrosis Quística
dc.subjectPolimorfismo Genético
dc.titleCFTR gene analysis in Latin American CF patients: heterogeneous origin and distribution of mutations across the continent
dc.typeArtículo


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