Jaouni, Tareq <br/><br/>
Association of pattern dystrophy with an HTRA1 single-nucleotide polymorphism.  [electronic resource] 

 -  Archives of ophthalmology (Chicago, Ill. : 1960)  Aug 2012 
 - 987-91 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1538-3601 
<br/><br/><label>Standard No.: </label>10.1001/archophthalmol.2012.1483  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Aged, 80 and over<br/>Bestrophins<br/>Chloride Channels--genetics<br/>Complement Factor H--genetics<br/>Cross-Sectional Studies<br/>Eye Proteins--genetics<br/>Female<br/>Fluorescein Angiography<br/>Genotype<br/>High-Temperature Requirement A Serine Peptidase 1<br/>Humans<br/>Intermediate Filament Proteins--genetics<br/>Male<br/>Membrane Glycoproteins--genetics<br/>Middle Aged<br/>Nerve Tissue Proteins--genetics<br/>Peripherins<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Polymorphism, Single Nucleotide<br/>Retinal Dystrophies--diagnosis<br/>Risk Factors<br/>Serine Endopeptidases--genetics<br/>Tomography, Optical Coherence<br/>Vitelliform Macular Dystrophy--diagnosis