Whole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness

A current focus in psychiatric genetics is detection of multiple common risk alleles through very large GWAS analyses. Yet families do exist, albeit rare, that have multiple affected members who are presumed to have a similar inherited cause to their illnesses. We hypothesized that within some of th...

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Detalles Bibliográficos
Autores principales: Homann, Oliver R, Misura, Kira, Lamas, Edwin, Sandrock, Robert W, Nelson, Paul, McDonough, Stefan I, DeLisi, Lynn E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5033653/
https://www.ncbi.nlm.nih.gov/pubmed/27001614
http://dx.doi.org/10.1038/mp.2016.24

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5033653/
https://www.ncbi.nlm.nih.gov/pubmed/27001614
http://dx.doi.org/10.1038/mp.2016.24

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