Xekouki, Paraskevi <br/><br/>
KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome.  [electronic resource] 

 -  Endocrine-related cancer  Jun 2012 
 - 255-60 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Intramural 
<br/><br/><label>ISSN: </label>1479-6821 
<br/><br/><label>Standard No.: </label>10.1530/ERC-12-0022  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenoma--genetics<br/>Cohort Studies<br/>DNA, Neoplasm--genetics<br/>Female<br/>G Protein-Coupled Inwardly-Rectifying Potassium Channels--physiology<br/>HEK293 Cells<br/>Humans<br/>Hyperaldosteronism--genetics<br/>Male<br/>Mutation<br/>National Institutes of Health (U.S.)<br/>United States