Author:
Pankow Sandra,Bamberger Casimir,Calzolari Diego,Martínez-Bartolomé Salvador,Lavallée-Adam Mathieu,Balch William E.,Yates John R.
Publisher
Springer Science and Business Media LLC
Reference55 articles.
1. Dalemans, W. et al. Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation. Nature 354, 526–528 (1991)
2. Collins, F. S. Cystic fibrosis: molecular biology and therapeutic implications. Science 256, 774–779 (1992)
3. Watson, M. S. et al. Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel. Genet. Med. 6, 387–391 (2004)
4. World Health Organization. The Molecular Genetic Epidemiology of Cystic Fibrosis
http://www.who.int/genomics/publications/en/HGN_WB_04.02_report.pdf
(World Health Organization, 2004)
5. Lukacs, G. L. et al. The ΔF508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells. J. Biol. Chem. 268, 21592–21598 (1993)
Cited by
227 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献