Carvajal, C A <br/><br/>
A de novo unequal cross-over mutation between CYP11B1 and CYP11B2 genes causes familial hyperaldosteronism type I.  [electronic resource] 

 -  Journal of endocrinological investigation  Feb 2011 
 - 140-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1720-8386 
<br/><br/><label>Standard No.: </label>10.1007/BF03347044  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Aged<br/>Aged, 80 and over<br/>Crossing Over, Genetic<br/>Cytochrome P-450 CYP11B2--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Humans<br/>Hyperaldosteronism--enzymology<br/>Male<br/>Middle Aged<br/>Mutation<br/>Pedigree<br/>Polymorphism, Genetic<br/>Steroid 11-beta-Hydroxylase--genetics