General and Specific Mechanisms of Visual Cognitive Function Impairment in People with FMRP Deficit

• Published in: Zurnal vyss̆ej nervnoj dejatelnosti imeni I P Pavlova Vol. 65; no. 3; p. 259
• Main Authors: Pereverzeva, D S, Danilina, K K, Gorbachevskaya, N L
• Format: Journal Article
• Language: Russian
• Published: Russia (Federation) 01.05.2015
• Subjects: Child Development Disorders, Pervasive - genetics; Child Development Disorders, Pervasive - physiopathology; Child Development Disorders, Pervasive - psychology; Cognition; Female; Fragile X Mental Retardation Protein - genetics; Fragile X Syndrome - genetics; Fragile X Syndrome - physiopathology; Fragile X Syndrome - psychology; Gene Expression; Humans; Male; Motion Perception; Mutation; Pattern Recognition, Visual

The purpose of this article is to provide the overview of visual cognitive development in subjects with FMRP deficit. Description of fragile X mental retardation syndrome is presented in the article, that is the most common cause of inherited intellectual disability and one of the most prevalent gen...