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Schizophrenia copy number variants and associative learning
Large-scale genomic studies have made major progress in identifying genetic risk variants for schizophrenia. A key finding from these studies is that there is an increased burden of genomic copy number variants (CNVs) in schizophrenia cases compared with controls. The mechanism through which these C...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Mol Psychiatry |
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| Κύριοι συγγραφείς: | , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Nature Publishing Group
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5285462/ https://ncbi.nlm.nih.gov/pubmed/27956746 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2016.227 |
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