Analysis of Cystic Fibrosis (cf) and Cftr Dysfunction Throughout the Lifespan
The clinical manifestation of cystic fibrosis (CF) is a result of mutation in the cystic fibrosis transmembrane conductance regulator (CFTR). At normal functioning, CFTR facilitates water movement and the transport of ions across the epithelial layer. Pulmonary pathogens attacking the lungs of an individual with...
