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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Elsevier,
2022-03-01T00:00:00Z.
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Internet
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