Cystic fibrosis (CF) is the most common lethal autosomal recessive genetic disorder that
affects the Caucasian population. CF is caused by mutations in the CF transmembrane …

The primary defect in cystic fibrosis (CF) is a result of mutations in the cystic fibrosis
transmembrane conductance regulator (CFTR) gene, which results in altered sodium and …

Cystic fibrosis, the most common inherited lethal disease in Caucasians, is caused by
mutations in the CF gene. The gene product, the CF transmembrane conductance regulator …

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) result in
defective ion transport, leading to thick mucus, impaired mucociliary clearance and …

Cystic fibrosis (CF), the most common life-threatening genetic disorder in Caucasians, is
caused by recessive mutations in the Cystic Fibrosis Transmembrane Regulator (CFTR) …

Cystic fibrosis (CF) is a genetic disorder caused by mutations in the gene encoding for the
cystic fibrosis transmembrane conductance regulator (CFTR) anion channel. Currently, more …

Cystic fibrosis (CF), the most common fatal monogenic disease in the United States, results
from mutations in CF transmembrane conductance regulator (CFTR), a chloride channel …

Cystic fibrosis is a common autosomal recessive disease caused by mutations in the CFTR
gene that encodes an anion channel expressed in epithelia and other cell types. While the …

Cystic fibrosis (CF) is an autosomal recessive genetic disorder caused by mutations in the
gene encoding for the anion channel cystic fibrosis transmembrane conductance regulator …

Chronic obstructive lung disease starting in the first months of life remains the major cause
of morbidity and mortality in patients with cystic fibrosis (CF). The discovery of the cystic …