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Identification and functional characterization of rare mutations of the neuroligin-2 gene (NLGN2) associated with schizophrenia

Schizophrenia is a severe chronic mental disorder with a high genetic component in its etiology. Several lines of study have suggested that synaptic dysfunction may underlie the pathogenesis of schizophrenia. Neuroligin proteins function as cell-adhesion molecules at post-synaptic membrane and play...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Sun, Chicheng, Cheng, Min-Chih, Qin, Rosie, Liao, Ding-Lieh, Chen, Tzu-Ting, Koong, Farn-Jong, Chen, Gong, Chen, Chia-Hsiang
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Oxford University Press 2011
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3131045/
https://ncbi.nlm.nih.gov/pubmed/21551456
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr208
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