Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia

The range of genetic variation with potential clinical implications in schizophrenia, beyond rare copy number variants (CNVs), remains uncertain. We therefore analyzed genome sequencing data for 259 unrelated adults with schizophrenia from a well-characterized community-based cohort previously exami...

Descripción completa

Detalles Bibliográficos
Autores principales: Mojarad, Bahareh A., Yin, Yue, Manshaei, Roozbeh, Backstrom, Ian, Costain, Gregory, Heung, Tracy, Merico, Daniele, Marshall, Christian R., Bassett, Anne S., Yuen, Ryan K. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851385/
https://www.ncbi.nlm.nih.gov/pubmed/33526774
http://dx.doi.org/10.1038/s41398-021-01211-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851385/
https://www.ncbi.nlm.nih.gov/pubmed/33526774
http://dx.doi.org/10.1038/s41398-021-01211-2

Ejemplares similares