Copyright
©The Author(s) 2015.
World J Crit Care Med. Aug 4, 2015; 4(3): 179-191
Published online Aug 4, 2015. doi: 10.5492/wjccm.v4.i3.179
Published online Aug 4, 2015. doi: 10.5492/wjccm.v4.i3.179
Figure 1 Classification of cystic fibrosis transmembrane conductance regulator mutations.
CFTR mutations are classified into six groups according to their effect on CFTR function. Class I mutations affect biosynthesis, while class II mutations affect protein processing. Milder mutations such as class II to Class V impair CFTR channel function. CFTR: Cystic fibrosis transmembrane conductance regulator.
- Citation: Reeves EP, McCarthy C, McElvaney OJ, Vijayan MSN, White MM, Dunlea DM, Pohl K, Lacey N, McElvaney NG. Inhaled hypertonic saline for cystic fibrosis: Reviewing the potential evidence for modulation of neutrophil signalling and function. World J Crit Care Med 2015; 4(3): 179-191
- URL: https://www.wjgnet.com/2220-3141/full/v4/i3/179.htm
- DOI: https://dx.doi.org/10.5492/wjccm.v4.i3.179