Khor, Chiea Chuen <br/><br/>
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.  [electronic resource] 

 -  Human molecular genetics  Dec 2013 
 - 5288-94 p.  digital 
<br/><br/> Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddt385  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Animals<br/>Gene Expression Regulation<br/>Genetic Predisposition to Disease<br/>Genome-Wide Association Study<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Mice<br/>Myopia--etiology<br/>Polymorphism, Single Nucleotide<br/>Repressor Proteins--genetics<br/>Retina--metabolism<br/>Sclera--metabolism<br/>Zinc Finger E-box Binding Homeobox 2