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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


Book ID
115466551
Publisher
Nature Publishing Group
Year
2012
Tongue
English
Weight
76 KB
Volume
44
Category
Article
ISSN
1061-4036

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