Cystic fibrosis with heterozygous f508del mutation in cftr gene
Cystic fibrosis (CF) is a genetic disorder characterized by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Among these mutations, the F508del variant
Cystic fibrosis (CF) is a genetic disorder characterized by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Among these mutations, the F508del variant