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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Mol Psychiatry
Prif Awduron: Clifton, N E, Pocklington, A J, Scholz, B, Rees, E, Walters, J T R, Kirov, G, O'Donovan, M C, Owen, M J, Wilkinson, L S, Thomas, K L, Hall, J
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group 2017
Pynciau:
Immediate Communication
Mynediad Ar-lein: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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