Bonny, Olivier <br/><br/>
A novel mutation of the epithelial Na+ channel causes type 1 pseudohypoaldosteronism.  [electronic resource] 

 -  Pediatric nephrology (Berlin, Germany)  Oct 2002 
 - 804-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0931-041X 
<br/><br/><label>Standard No.: </label>10.1007/s00467-002-0945-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aldosterone--blood<br/>Animals<br/>Exons--genetics<br/>Female<br/>Frameshift Mutation--genetics<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Mutation--genetics<br/>Oocytes--metabolism<br/>Pedigree<br/>Potassium--blood<br/>Pseudohypoaldosteronism--etiology<br/>Renin--blood<br/>Sodium--blood