Sumaroka, Alexander <br/><br/>
Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial Intelligence.  [electronic resource] 

 -  Investigative ophthalmology & visual science  06 2019 
 - 2551-2562 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-5783 
<br/><br/><label>Standard No.: </label>10.1167/iovs.19-27156  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Antigens, Neoplasm--genetics<br/>Calmodulin-Binding Proteins--genetics<br/>Cell Cycle Proteins<br/>Color Vision Defects--genetics<br/>Cytoskeletal Proteins<br/>Female<br/>Genetic Therapy<br/>Humans<br/>Leber Congenital Amaurosis--genetics<br/>Machine Learning<br/>Male<br/>Middle Aged<br/>Mutation<br/>Neoplasm Proteins--genetics<br/>Retinal Cone Photoreceptor Cells--physiology<br/>Retinitis Pigmentosa--genetics<br/>Tomography, Optical Coherence--methods<br/>Visual Field Tests<br/>Visual Fields--physiology<br/>Young Adult