Visual sensorial impairments in neurodevelopmental disorders: evidence for a retinal phenotype in Fragile X Syndrome.
Rossignol, Rafaëlle
Visual sensorial impairments in neurodevelopmental disorders: evidence for a retinal phenotype in Fragile X Syndrome. [electronic resource] - PloS one 2014 - e105996 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1932-6203
10.1371/journal.pone.0105996 doi
Animals
Disease Models, Animal
Fragile X Mental Retardation Protein--genetics
Fragile X Syndrome--genetics
Male
Mice
Mice, Knockout
Phenotype
Retina--metabolism
Rhodopsin--genetics
Visual Perception--physiology
Visual sensorial impairments in neurodevelopmental disorders: evidence for a retinal phenotype in Fragile X Syndrome. [electronic resource] - PloS one 2014 - e105996 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1932-6203
10.1371/journal.pone.0105996 doi
Animals
Disease Models, Animal
Fragile X Mental Retardation Protein--genetics
Fragile X Syndrome--genetics
Male
Mice
Mice, Knockout
Phenotype
Retina--metabolism
Rhodopsin--genetics
Visual Perception--physiology