Characterization of CFTR chloride channel
Cystic fibrosis (CF) is an inherited disease caused by mutations in a single gene which encodes the cystic fibrosis transmembrane conductance regulator (CFTR), a member of ATP-binding cassette (ABC) proteins superfamily. Since the genetic basis of CF was resolved in 1989 when the CFTR gene was clone...
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| Format: | Thesis |
| Language: | English |
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2009
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| Online Access: | https://hdl.handle.net/10356/19294 |