[De novo mutations in SYNGAP1 associated with non-syndromic mental retardation]

MeSH terms

• Animals
• Child
• Cognition Disorders / genetics
• GTPase-Activating Proteins / genetics*
• Humans
• Intellectual Disability / genetics*
• Learning Disabilities / genetics
• Memory Disorders / genetics
• Mice
• Mice, Knockout
• Models, Neurological
• Neuronal Plasticity / genetics
• Point Mutation*
• Receptors, N-Methyl-D-Aspartate / physiology
• Signal Transduction / genetics
• Signal Transduction / physiology
• Synaptic Transmission / genetics
• Synaptic Transmission / physiology
• ras GTPase-Activating Proteins / deficiency
• ras GTPase-Activating Proteins / genetics