Diagnostic contribution of molecular analysis of the cystic fibrosis transmembrane conductance regulator gene in patients suspected of having mild or atypical cystic fibrosis

OBJECTIVE: To evaluate the diagnostic contribution of molecular analysis of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in patients suspected of having mild or atypical cystic fibrosis (CF). METHODS: This was a cross-sectional study involving adolescents and adults aged ≥ 14...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Dal'Maso, Vinícius Buaes, Mallmann, Lucas, Siebert, Marina, Simon, Laura, Saraiva-Pereira, Maria Luiza, Dalcin, Paulo de Tarso Roth
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Sociedade Brasileira de Pneumologia e Tisiologia 2013
Θέματα:
Original Article
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4075816/
https://ncbi.nlm.nih.gov/pubmed/23670503
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/S1806-37132013000200009
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