Delaney, S J <br/><br/>
Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels.  [electronic resource] 

 -  Nature genetics  Aug 1993 
 - 426-31 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/ng0893-426  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alternative Splicing<br/>Amino Acid Sequence<br/>Animals<br/>Base Sequence<br/>Chloride Channels--genetics<br/>Conserved Sequence<br/>Cystic Fibrosis--genetics<br/>Cystic Fibrosis Transmembrane Conductance Regulator<br/>Exons<br/>Genetic Variation<br/>Humans<br/>Introns<br/>Membrane Proteins--genetics<br/>Mice<br/>Molecular Sequence Data<br/>Mutagenesis, Site-Directed<br/>Oligodeoxyribonucleotides<br/>Organ Specificity<br/>Polymerase Chain Reaction<br/>Restriction Mapping