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pro vyhledávání: '"Ahmad Alodib"'
Autor:
Khalid M. Sumaily, Refat Nimer, Maha Alzahrani, Mai Abdel Jabar, Ahmad Alodib, Essa M. Sabi, Imran Nizami, Anas M. Abdel Rahman
Publikováno v:
Journal of pharmaceutical and biomedical analysis. 216
The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel found on the apical surface of epithelial cells in the airway and gastrointestinal tract. A mutation in the CFTR protein is responsible for developing cystic fibrosi