Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures

Genomic copy number variants (CNVs) are amongst the most highly penetrant genetic risk factors for neuropsychiatric disorders. The scarcity of carriers of individual CNVs and their phenotypical heterogeneity limits investigations of the associated neural mechanisms and endophenotypes. We applied a n...

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Detalles Bibliográficos
Autores principales: Drakesmith, Mark, Parker, Greg D., Smith, Jacqueline, Linden, Stefanie C., Rees, Elliott, Williams, Nigel, Owen, Michael J., van den Bree, Marianne, Hall, Jeremy, Jones, Derek K., Linden, David E. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389944/
https://www.ncbi.nlm.nih.gov/pubmed/30804328
http://dx.doi.org/10.1038/s41398-019-0440-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389944/
https://www.ncbi.nlm.nih.gov/pubmed/30804328
http://dx.doi.org/10.1038/s41398-019-0440-7

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