Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

Evidence for the etiology of autism spectrum disorders (ASD) has consistently pointed to a strong genetic component complicated by substantial locus heterogeneity(1,2). We sequenced the exomes of 20 sporadic cases of ASD and their parents, reasoning that these families would be enriched for de novo...

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Detalles Bibliográficos
Autores principales: O’Roak, Brian J., Deriziotis, Pelagia, Lee, Choli, Vives, Laura, Schwartz, Jerrod J., Girirajan, Santhosh, Karakoc, Emre, MacKenzie, Alexandra P., Ng, Sarah B., Baker, Carl, Rieder, Mark J., Nickerson, Deborah A., Bernier, Raphael, Fisher, Simon E., Shendure, Jay, Eichler, Evan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115696/
https://www.ncbi.nlm.nih.gov/pubmed/21572417
http://dx.doi.org/10.1038/ng.835

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115696/
https://www.ncbi.nlm.nih.gov/pubmed/21572417
http://dx.doi.org/10.1038/ng.835

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