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Exome sequencing supports a de novo mutational paradigm for schizophrenia

Despite high heritability, a large fraction of cases with schizophrenia do not have a family history of the disease (sporadic cases). Here, we examine the possibility that rare de novo protein-altering mutations contribute to the genetic component of schizophrenia by sequencing the exome of 53 spora...

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Detalles Bibliográficos
Autores principales: Xu, Bin, Roos, J. Louw, Dexheimer, Phillip, Boone, Braden, Plummer, Brooks, Levy, Shawn, Gogos, Joseph A., Karayiorgou, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196550/
https://www.ncbi.nlm.nih.gov/pubmed/21822266
http://dx.doi.org/10.1038/ng.902