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Home > Modelling Cystic Fibrosis Disease Progression in Patients with the Rare CFTR Mutation P67L

Modelling Cystic Fibrosis Disease Progression in Patients with the Rare CFTR Mutation P67L

Resource Type

CF Research News

Authors

Isobel E.R. MacKenzie, Valerie Paquette, Frances Gosse, Sheenagh George, Frederic Chappe and Valerie Chappe

References

J Cyst Fibros. 2017 May;16(3):335-341.

Document

PDF icon CF Research News Article [1]

Link

Scientific Abstract [2]

Keywords

Data Registry [3]
Disease progression [4]
Mild CF [5]
P67L [6]
Rare mutations [7]

Date

Tuesday, May 16, 2017

Featured resource article

Yes

Resource - Guideline Type

Other Guidelines [8]
Source URL:https://www.ecfs.eu/resource-article/cf-research-news/modelling-cystic-fibrosis-disease-progression-patients-rare-cftr

Links
[1] https://www.ecfs.eu/sites/default/files/cf-research-article-files/JCF-D-16-003381R1_FINAL_Chappe_14052017.pdf [2] https://www.ncbi.nlm.nih.gov/pubmed/28392015 [3] https://www.ecfs.eu/research-article-keywords/data-registry [4] https://www.ecfs.eu/research-article-keywords/disease-progression [5] https://www.ecfs.eu/research-article-keywords/mild-cf [6] https://www.ecfs.eu/research-article-keywords/p67l [7] https://www.ecfs.eu/research-article-keywords/rare-mutations [8] https://www.ecfs.eu/resource-guideline-type/other-guidelines