Genetic and phenotypic traits of children and adolescents with cystic fibrosis in Southern Brazil

OBJECTIVES: To characterize the main identified mutations on cystic fibrosis transmembrane conductance regulator (CFTR) in a group of children and adolescents at a cystic fibrosis center and its association with the clinical and laboratorial characteristics. METHOD: Descriptive cross-sectional study...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Bras Pneumol
Prif Awduron: da Rosa, Katiana Murieli, de Lima, Eliandra da Silveira, Machado, Camila Correia, Rispoli, Thaiane, Silveira, Victória d’Azevedo, Ongaratto, Renata, Comaru, Talitha, Pinto, Leonardo Araújo
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Sociedade Brasileira de Pneumologia e Tisiologia 2018
Pynciau:
Original Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6459751/
https://ncbi.nlm.nih.gov/pubmed/30726326
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/s1806-37562017000000418
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