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

✍ Scribed by 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

Book ID: 118675991
Publisher: Nature Publishing Group
Year: 2011
Tongue: English
Weight: 596 KB
Volume: 43
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng.835

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