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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...
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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2011
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| Témata: | |
| On-line přístup: | 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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