Corrigendum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (Nature Genetics (2011) 43, (585-589))

Brian O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J. Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P. MacKenzie, Sarah B. Ng, Carl Baker, Mark J. Rieder, Deborah A. Nickerson, Raphael Bernier, Simon E. Fisher, Jay Shendure, Evan E. Eichler

Research output: Contribution to journalArticle

10 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)471
Number of pages1
JournalNature Genetics
Volume44
Issue number4
DOIs
StatePublished - Apr 2012
Externally publishedYes

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Exome
Mutation
corrigendum
Autism Spectrum Disorder

ASJC Scopus subject areas

  • Genetics

Cite this

Corrigendum : Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (Nature Genetics (2011) 43, (585-589)). / O'Roak, Brian; 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.

In: Nature Genetics, Vol. 44, No. 4, 04.2012, p. 471.

Research output: Contribution to journalArticle

O'Roak, B, 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 2012, 'Corrigendum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (Nature Genetics (2011) 43, (585-589))', Nature Genetics, vol. 44, no. 4, pp. 471. https://doi.org/10.1038/ng0412-471
O'Roak, Brian ; 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. / Corrigendum : Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (Nature Genetics (2011) 43, (585-589)). In: Nature Genetics. 2012 ; Vol. 44, No. 4. pp. 471.
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