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

CONCLUSIONS: Genetic and molecular characterization of PwCF poses an important step not just for CF diagnosis and prognosis which is tightly correlated with the clinical phenotype, but also for the eligibility of CFTR modulator drugs.PMID:34252371 | DOI:10.1016/j.jped.2021.05.010

Source: Jornal de Pediatria - July 12, 2021 Category: Pediatrics Authors: Juliana Roda Teresa Teixeira Iris Ai Silva Teresa Reis Silva Ricardo Ferreira Margarida D Amaral Guiomar Oliveira Source Type: research