Clinical and molecular characterization of the R751L-CFTR mutation.
CFTR mutations
R751L
cystic fibrosis
primary airway epithelial cells
Journal
American journal of physiology. Lung cellular and molecular physiology
ISSN: 1522-1504
Titre abrégé: Am J Physiol Lung Cell Mol Physiol
Pays: United States
ID NLM: 100901229
Informations de publication
Date de publication:
01 02 2021
01 02 2021
Historique:
pubmed:
10
12
2020
medline:
24
3
2021
entrez:
9
12
2020
Statut:
ppublish
Résumé
Cystic fibrosis (CF) arises from mutations in the CF transmembrane conductance regulator (
Identifiants
pubmed: 33296276
doi: 10.1152/ajplung.00137.2020
pmc: PMC8476205
doi:
Substances chimiques
CFTR protein, human
0
Cystic Fibrosis Transmembrane Conductance Regulator
126880-72-6
Sodium Chloride
451W47IQ8X
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
L288-L300Subventions
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M008797/1
Pays : United Kingdom
Organisme : Medical Research Council (MRC)
ID : MR/M008797/1
Organisme : Wellcome Trust (Wellcome)
ID : 203520/Z/16/Z
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