Defective Ion Channel in Cystic Fibrosis: Current Development in Treatment of Cystic Fibrosis
Ngoga Godfrey, M. M. Ganyam, G.O. Ibiang, C. A. Difa & Nelson Christian · Asian Journal of Biochemistry, Genetics and Molecular Biology · 2020
Cystic fibrosis is an inherited disorder that causes severe damage to the lungs, digestive system and other organs in the body. Cystic fibrosis transmembrane conductance regulator (CFTR) is involved in the production of mucus, sweat and digestive juices. These secreted fluids are...
Open access
Research Article
10.9734/ajbgmb/2020/v4i130099