Cipriani, Valentina <br/><br/>
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.  [electronic resource] 

 -  Human molecular genetics  Sep 2012 
 - 4138-50 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/dds225  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Aged, 80 and over<br/>Case-Control Studies<br/>Chromosomes, Human, Pair 6<br/>Female<br/>Genetic Loci<br/>Genetic Predisposition to Disease<br/>Genome-Wide Association Study<br/>Haplotypes<br/>Humans<br/>Immunophilins--genetics<br/>Linear Models<br/>Logistic Models<br/>Macular Degeneration--genetics<br/>Male<br/>Odds Ratio<br/>Polymorphism, Single Nucleotide<br/>Principal Component Analysis<br/>Proto-Oncogene Proteins--genetics<br/>Receptor, Notch4<br/>Receptors, Notch--genetics<br/>Sequence Analysis, DNA<br/>Tacrolimus Binding Proteins<br/>Tenascin--genetics