Molecular mechanism of anion permeation through CFTR channel pore
Cystic fibrosis is an inherited disease caused by mutations in a single gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR), a member of ATP-binding cassette (ABC) proteins superfamily. Several approaches have been applied to determine the pore-lining domains or residues inc...
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| Format: | Thesis |
| Language: | English |
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2009
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| Online Access: | https://hdl.handle.net/10356/19012 |