Canfield, M C <br/><br/>
Identification and characterization of aquaporin-2 water channel mutations causing nephrogenic diabetes insipidus with partial vasopressin response.  [electronic resource] 

 -  Human molecular genetics  Oct 1997 
 - 1865-71 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/6.11.1865  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Aquaporin 2<br/>Aquaporin 6<br/>Aquaporins<br/>CHO Cells<br/>Cricetinae<br/>DNA Mutational Analysis<br/>Deamino Arginine Vasopressin--therapeutic use<br/>Diabetes Insipidus, Nephrogenic--drug therapy<br/>Female<br/>Humans<br/>Hypoglycemic Agents--therapeutic use<br/>Ion Channels--genetics<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Pedigree