Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels. [electronic resource]
Producer: 19931105Description: 426-31 p. digitalISSN:- 1061-4036
- Alternative Splicing
- Amino Acid Sequence
- Animals
- Base Sequence
- Chloride Channels -- genetics
- Conserved Sequence
- Cystic Fibrosis -- genetics
- Cystic Fibrosis Transmembrane Conductance Regulator
- Exons
- Genetic Variation
- Humans
- Introns
- Membrane Proteins -- genetics
- Mice
- Molecular Sequence Data
- Mutagenesis, Site-Directed
- Oligodeoxyribonucleotides
- Organ Specificity
- Polymerase Chain Reaction
- Restriction Mapping
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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