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Screening for F508del as a first step in the molecular diagnosis of cystic fibrosis,
OBJECTIVE: To determine the relevance of screening for the F508del mutation of the cystic fibrosis transmembrane conductance regulator gene as a first step in the genetic diagnosis of cystic fibrosis (CF) by associating the genotype with various clinical variables. METHODS: We evaluated 180 CF patie...
Autores principales: | Marson, Fernando Augusto de Lima, Bertuzzo, Carmen Silvia, Ribeiro, Maria Ângela Gonçalves de Oliveira, Ribeiro, Antônio Fernando, Ribeiro, José Dirceu |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Pneumologia e Tisiologia
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075852/ https://www.ncbi.nlm.nih.gov/pubmed/23857699 http://dx.doi.org/10.1590/S1806-37132013000300007 |
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