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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Mol Psychiatry
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2017
Assuntos:
Immediate Communication
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados