Guaragna, Mara S <br/><br/>
Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuria.  [electronic resource] 

 -  Biochemical and biophysical research communications  Nov 2013 
 - 371-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-2104 
<br/><br/><label>Standard No.: </label>10.1016/j.bbrc.2013.10.064  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Exons--genetics<br/>Female<br/>Humans<br/>Molecular Sequence Data<br/>Mutation<br/>Nephrosis--complications<br/>Pedigree<br/>Protein Conformation<br/>Proteinuria--etiology<br/>WT1 Proteins--chemistry<br/>Young Adult