Cargando…
A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband
Schizophrenia is a debilitating mental disorder affecting approximately 1% of the world's population. Childhood onset schizophrenia (COS), defined as onset before age 13, is a rare and severe form of the illness that may have more salient genetic influence. We identified a ~134 kb duplication s...
Autores principales: | Wilson, Nicole K. A., Lee, Yohan, Long, Robert, Hermetz, Karen, Rudd, M. Katharine, Miller, Rachel, Rapoport, Judith L., Addington, Anjené M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447216/ https://www.ncbi.nlm.nih.gov/pubmed/23074677 http://dx.doi.org/10.1155/2011/585893 |
Ejemplares similares
-
The human-specific paralogs SRGAP2B and SRGAP2C differentially modulate SRGAP2A-dependent synaptic development
por: Schmidt, Ewoud R. E., et al.
Publicado: (2019) -
Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders
por: Kokkonen, Hannaleena, et al.
Publicado: (2021) -
Structural History of Human SRGAP2 Proteins
por: Sporny, Michael, et al.
Publicado: (2017) -
Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3
por: Blazejewski, Sara M., et al.
Publicado: (2018) -
Microduplications of 16p11.2 are Associated with Schizophrenia
por: McCarthy, Shane, et al.
Publicado: (2009)