Rare loss of function mutations in N-methyl-d-aspartate glutamate receptors and their contributions to schizophrenia susceptibility

In schizophrenia (SCZ) and autism spectrum disorder (ASD), the dysregulation of glutamate transmission through N-methyl-d-aspartate receptors (NMDARs) has been implicated as a potential etiological mechanism. Previous studies have accumulated evidence supporting NMDAR-encoding genes' role in et...

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Detalles Bibliográficos
Autores principales: Yu, Yanjie, Lin, Yingni, Takasaki, Yuto, Wang, Chenyao, Kimura, Hiroki, Xing, Jingrui, Ishizuka, Kanako, Toyama, Miho, Kushima, Itaru, Mori, Daisuke, Arioka, Yuko, Uno, Yota, Shiino, Tomoko, Nakamura, Yukako, Okada, Takashi, Morikawa, Mako, Ikeda, Masashi, Iwata, Nakao, Okahisa, Yuko, Takaki, Manabu, Sakamoto, Shinji, Someya, Toshiyuki, Egawa, Jun, Usami, Masahide, Kodaira, Masaki, Yoshimi, Akira, Oya-Ito, Tomoko, Aleksic, Branko, Ohno, Kinji, Ozaki, Norio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802496/
https://www.ncbi.nlm.nih.gov/pubmed/29317596
http://dx.doi.org/10.1038/s41398-017-0061-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802496/
https://www.ncbi.nlm.nih.gov/pubmed/29317596
http://dx.doi.org/10.1038/s41398-017-0061-y

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