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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, CarlVolume:
44
Year:
2012
Language:
english
Pages:
1
DOI:
10.1038/ng0412-471
File:
PDF, 76 KB
english, 2012