Genetic modification of cystic fibrosis with ΔF508 mutation of CFTR gene using the CRISPR system in peripheral blood mononuclear cells
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DOI: 10.22038/ijbms.2020.50051.11415
Abstract: Objective(s): Cystic fibrosis (CF) is an inherited autosomal recessive disease that is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The present study aimed to investigate the genetic modification of CF… read more here.
Keywords: cystic fibrosis; f508 mutation; cftr gene; mutation cftr ... See more keywords