Cascavilla, Maria Lucia <br/><br/>
Unilateral vitelliform phenotype in autosomal recessive bestrophinopathy.  [electronic resource] 

 -  Ophthalmic research  2012 
 - 146-50 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1423-0259 
<br/><br/><label>Standard No.: </label>10.1159/000338750  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age of Onset<br/>Bestrophins<br/>Child<br/>Chloride Channels--genetics<br/>Electrooculography<br/>Electroretinography<br/>Eye Proteins--genetics<br/>Female<br/>Fluorescein Angiography<br/>Humans<br/>Mutation<br/>Phenotype<br/>Severity of Illness Index<br/>Tomography, Optical Coherence<br/>Vitelliform Macular Dystrophy--diagnosis