Rossignol, Rafaëlle <br/><br/>
Visual sensorial impairments in neurodevelopmental disorders: evidence for a retinal phenotype in Fragile X Syndrome.  [electronic resource] 

 -  PloS one  2014 
 - e105996 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0105996  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Disease Models, Animal<br/>Fragile X Mental Retardation Protein--genetics<br/>Fragile X Syndrome--genetics<br/>Male<br/>Mice<br/>Mice, Knockout<br/>Phenotype<br/>Retina--metabolism<br/>Rhodopsin--genetics<br/>Visual Perception--physiology