No abstract available
MeSH terms
-
Cystic Fibrosis / drug therapy*
-
Cystic Fibrosis / genetics
-
Cystic Fibrosis Transmembrane Conductance Regulator / chemistry
-
Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
-
Gene Expression Regulation
-
Humans
-
Molecular Chaperones / physiology
-
Mutation*
-
Protein Conformation*
Substances
-
CFTR protein, human
-
Molecular Chaperones
-
Cystic Fibrosis Transmembrane Conductance Regulator