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Pediatric population with cystic fibrosis in the centre of Portugal: candidates for new therapies

OBJECTIVES: Cystic fibrosis (CF) is a severe autosomal recessive disease that results from mutations in a gene encoding the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein, a chloride channel. This study aims to characterize the clinical and genetic features of a cohort of pediatr...

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Detalles Bibliográficos
Autores principales:	Roda, Juliana, Teixeira, Teresa, AI Silva, Iris, Silva, Teresa Reis, Ferreira, Ricardo, Amaral, Margarida D., Oliveira, Guiomar
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2021
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9432345/ https://www.ncbi.nlm.nih.gov/pubmed/34252371 http://dx.doi.org/10.1016/j.jped.2021.05.010

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