Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis

Medicine & Life Sciences

• African Americans 9%
• Cystic Fibrosis 77%
• Cystic Fibrosis Transmembrane Conductance Regulator 100%
• DNA 5%
• Epithelial Cells 56%
• Gene Expression 5%
• Genes 16%
• Heterozygote 21%
• Homozygote 10%
• Lung 5%
• Lung Diseases 8%
• Messenger RNA 45%
• Mutation 16%
• Nonsense Codon 90%
• Nose 16%
• Pancreas 8%
• Pancreatic Diseases 12%
• Polymerase Chain Reaction 5%
• Population 3%
• Proteins 3%