Prevalence of ΔF508 mutation in the cystic fibrosis transmembrane conductance regulator gene among cystic fibrosis patients from a Brazilian referral center

To verify the presence of ΔF508 mutation in the cystic fibrosis transmembrane conductance regulator gene among patients with cystic fibrosis diagnosed by the sweat test for sodium and chlorine and followed at the Pediatric Pneumology Outpatient Clinic of Universidade Estadual de Campinas, Brazil, a...

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Veröffentlicht in:	Jornal de pediatria 2012-11, Vol.88 (6), p.531-4
Hauptverfasser:	Bieger, Andréia Marisa, Marson, Fernando Augusto de Lima, Bertuzzo, Carmen Sílvia
Format:	Artikel
Sprache:	eng
Schlagworte:	Alleles Brazil - ethnology Cystic Fibrosis - ethnology Cystic Fibrosis - genetics Cystic Fibrosis Transmembrane Conductance Regulator - genetics European Continental Ancestry Group - ethnology Genotype Humans Mutation - genetics Polymerase Chain Reaction Referral and Consultation
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