Sheppard, D N <br/><br/>
Understanding how cystic fibrosis mutations cause a loss of Cl- channel function.  [electronic resource] 

 -  Molecular medicine today  Jul 1996 
 - 290-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review 
<br/><br/><label>ISSN: </label>1357-4310 
<br/><br/><label>Standard No.: </label>10.1016/1357-4310(96)10028-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chlorides--metabolism<br/>Cystic Fibrosis--genetics<br/>Cystic Fibrosis Transmembrane Conductance Regulator--genetics<br/>Genotype<br/>Humans<br/>Models, Molecular<br/>Mutation<br/>Patch-Clamp Techniques