Cystic fibrosis, a multi-systemic mucosal disease: 25 years after the discovery of CFTR

Int J Biochem Cell Biol. 2014 Jul:52:2-4. doi: 10.1016/j.biocel.2014.04.006. Epub 2014 Apr 13.

Authors

Aleksander Edelman¹, Jean-Michel Sallenave²

Affiliations

¹ INSERM, U1151, Paris, France; Faculté de Médecine, Université Paris Descartes, Paris, France.
² INSERM, UMR1152, Paris, France; University Paris Diderot, Sorbonne Paris Cité, Paris, France. Electronic address: [email protected].

PMID: 24735713
DOI: 10.1016/j.biocel.2014.04.006

No abstract available

Publication types

Editorial

MeSH terms

Animals
Cystic Fibrosis / genetics*
Cystic Fibrosis / physiopathology*
Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
Humans

Substances

Cystic Fibrosis Transmembrane Conductance Regulator