Case Report: A Novel De Novo Missense Mutation of the GRIA2 Gene in a Chinese Case of Neurodevelopmental Disorder With Language Impairment

Biochemistry, Genetics and Molecular Biology

• Missense Mutation 100%
• GRIA2 100%
• Exome Sequencing 50%
• Ionotropic Receptor 16%
• Amino Methyl Phosphonic Acid 16%
• Ionotropic Glutamate Receptor 16%
• Gene Mutation 16%
• Mental Development 16%