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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Immediate Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5285462/
https://www.ncbi.nlm.nih.gov/pubmed/27956746
http://dx.doi.org/10.1038/mp.2016.227

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5285462/
https://www.ncbi.nlm.nih.gov/pubmed/27956746
http://dx.doi.org/10.1038/mp.2016.227

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