Human GRIN2B variants in neurodevelopmental disorders

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...

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Detalles Bibliográficos
Autores principales: Hu, Chun, Chen, Wenjuan, Myers, Scott J., Yuan, Hongjie, Traynelis, Stephen F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5125235/
https://www.ncbi.nlm.nih.gov/pubmed/27818011
http://dx.doi.org/10.1016/j.jphs.2016.10.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5125235/
https://www.ncbi.nlm.nih.gov/pubmed/27818011
http://dx.doi.org/10.1016/j.jphs.2016.10.002

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