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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Main Authors: Juliana Roda (Author), Teresa Teixeira (Author), Iris AI Silva (Author), Teresa Reis Silva (Author), Ricardo Ferreira (Author), Margarida D. Amaral (Author), Guiomar Oliveira (Author)
Format: Book
Published: Elsevier, 2022-03-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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