Common alleles contribute to schizophrenia in CNV carriers

The genetic architecture of schizophrenia is complex, involving risk alleles ranging from common alleles of weak effect to rare alleles of large effect, the best exemplar of the latter being large copy number variants (CNVs). It is currently unknown whether pathophysiology in those with defined rare...

Descripción completa

Detalles Bibliográficos
Autores principales: Tansey, K E, Rees, E, Linden, D E, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, P, Kirov, G, Walters, J, Owen, M J, O'Donovan, M C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960448/
https://www.ncbi.nlm.nih.gov/pubmed/26390827
http://dx.doi.org/10.1038/mp.2015.143

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960448/
https://www.ncbi.nlm.nih.gov/pubmed/26390827
http://dx.doi.org/10.1038/mp.2015.143

Ejemplares similares