Bakir-Gungor, Burcu <br/><br/>
Identification of possible pathogenic pathways in Behçet's disease using genome-wide association study data from two different populations.  [electronic resource] 

 -  European journal of human genetics : EJHG  May 2015 
 - 678-87 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2014.158  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Behcet Syndrome--diagnosis<br/>Computational Biology--methods<br/>Databases, Genetic<br/>Datasets as Topic<br/>Genetic Predisposition to Disease<br/>Genome-Wide Association Study<br/>Humans<br/>Japan<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Signal Transduction<br/>Turkey