Ostedgaard, L. S., Zabner, J., Vermeer, D. W., Rokhlina, T., Karp, P. H., Stecenko, A. A., . . . Welsh, M. J. (2002). CFTR with a partially deleted R domain corrects the cystic fibrosis chloride transport defect in human airway epithelia in vitro and in mouse nasal mucosa in vivo. The National Academy of Sciences.
Citação norma ChicagoOstedgaard, Lynda S., Joseph Zabner, Daniel W. Vermeer, Tatiana Rokhlina, Philip H. Karp, Arlene A. Stecenko, Christoph Randak, and Michael J. Welsh. CFTR With a Partially Deleted R Domain Corrects the Cystic Fibrosis Chloride Transport Defect in Human Airway Epithelia in Vitro and in Mouse Nasal Mucosa in Vivo. The National Academy of Sciences, 2002.
ציטוט MLAOstedgaard, Lynda S., et al. CFTR With a Partially Deleted R Domain Corrects the Cystic Fibrosis Chloride Transport Defect in Human Airway Epithelia in Vitro and in Mouse Nasal Mucosa in Vivo. The National Academy of Sciences, 2002.