Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
O'Roak BJ; Deriziotis P; Lee C; Vives L; Schwartz JJ; Girirajan S; Karakoc E; Mackenzie AP; Ng SB; Baker C; Rieder MJ; Nickerson DA; Bernier R; Fisher SE; Shendure J; Eichler EE; Nature Genetics, 2011, vol. 43, issue 6, p 585, ISSN 15461718. ISBN 15461718.

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