Piret, Sian E <br/><br/>
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21.  [electronic resource] 

 -  Human genetics  Jan 2011 
 - 51-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-1203 
<br/><br/><label>Standard No.: </label>10.1007/s00439-010-0897-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 2--genetics<br/>Female<br/>Genetic Heterogeneity<br/>Genetic Linkage<br/>Genetic Loci<br/>Genetic Predisposition to Disease<br/>Genome, Human<br/>Genome-Wide Association Study<br/>Gout--genetics<br/>Humans<br/>Hyperuricemia--genetics<br/>Kidney Diseases--genetics<br/>Kidney Failure, Chronic--genetics<br/>Male<br/>Pedigree<br/>Uric Acid--blood