Human GRIN2B variants in neurodevelopmental disorders

• Ngā kaituhi matua: Chun Hu (Author), Wenjuan Chen (Author), Scott J. Myers (Author), Hongjie Yuan (Author), Stephen F. Traynelis (Author)
• Hōputu: Pukapuka
• I whakaputaina: Elsevier, 2016-10-01T00:00:00Z.
• Ngā marau: article
• Urunga tuihono: Connect to this object online.

The development of whole exome/genome sequencing technologies has given rise to an unprecedented volume of data linking patient genomic variability to brain disorder phenotypes. A surprising number of variants have been found in the N-methyl-d-aspartate receptor (NMDAR) gene family, with the GRIN2B...