The ΔF508 Mutation Disrupts Packing of the Transmembrane Segments of the Cystic Fibrosis Transmembrane Conductance Regulator
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference58 articles.
1. Epithelial Cell Dysfunction in Cystic Fibrosis: Implications for Airways Disease
2. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
3. Therapeutic approaches to repair defects in ΔF508 CFTR folding and cellular targeting
4. The Phenotypic Consequences of CFTR Mutations
5. Cystic Fibrosis Transmembrane Conductance Regulator Has an Altered Structure When Its Maturation Is Inhibited1
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