Human GRIN2B variants in neurodevelopmental disorders

• मुख्य लेखकों: Chun Hu (लेखक), Wenjuan Chen (लेखक), Scott J. Myers (लेखक), Hongjie Yuan (लेखक), Stephen F. Traynelis (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Elsevier, 2016-10-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: 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...