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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
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.
Affiliation
  • O'Roak BJ; Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington, USA.
Nat Genet ; 43(6): 585-9, 2011 Jun.
Article in En | MEDLINE | ID: mdl-21572417
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Child Development Disorders, Pervasive / Genetic Predisposition to Disease / Mutation Limits: Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 2011 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Child Development Disorders, Pervasive / Genetic Predisposition to Disease / Mutation Limits: Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 2011 Document type: Article Affiliation country: