Novel rare variations in genes that regulate developmental change in N-methyl-d-aspartate receptor in patients with schizophrenia

The mechanism underlying the vulnerability to developing schizophrenia (SCZ) during adolescence remains elusive. Hypofunction of N -methyl- d -aspartate receptors (NMDARs) has been implicated in the pathophysiology of SCZ. During development, the composition of synaptic NMDARs dramatically changes f...

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Veröffentlicht in:	Human genome variation 2018-02, Vol.5 (1), p.17056-17056, Article 17056
Hauptverfasser:	Yoshikawa, Akane, Nishimura, Fumichika, Inai, Aya, Eriguchi, Yosuke, Nishioka, Masaki, Takaya, Atsuhiko, Tochigi, Mamoru, Kawamura, Yoshiya, Umekage, Tadashi, Kato, Kayoko, Sasaki, Tsukasa, Kasai, Kiyoto, Kakiuchi, Chihiro
Format:	Artikel
Sprache:	eng
Schlagworte:	631/208/135 631/378/2583 Biomedical and Life Sciences Biomedicine Gene Expression Gene Function Gene Therapy Human Genetics Molecular Medicine Schizophrenia
Online-Zugang:	Volltext
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