Johansen, Christopher T <br/><br/>
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.  [electronic resource] 

 -  Nature genetics  Aug 2010 
 - 684-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1546-1718 
<br/><br/><label>Standard No.: </label>10.1038/ng.628  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing<br/>Adult<br/>Apolipoprotein A-V<br/>Apolipoproteins A<br/>Cohort Studies<br/>Female<br/>Genes<br/>Genetic Testing<br/>Genetic Variation<br/>Genome-Wide Association Study<br/>Humans<br/>Hypertriglyceridemia--genetics<br/>Lipids--blood<br/>Lipoprotein Lipase<br/>Male<br/>Middle Aged<br/>Phenotype