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

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

doi:10.1038/ng.835

Keywords

BiologyExome sequencingGeneticsMissense mutationExomeProbandLocus (genetics)AutismGenetic heterogeneityMutationGenePhenotypeMedicine

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Publication Info

Year: 2011
Type: article
Volume: 43
Issue: 6
Pages: 585-589
Citations: 1202
Access: Closed

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APA Style

                            
                                
                                    Brian J. O’Roak, 
                                
                                    Pelagia Deriziotis, 
                                
                                    Choli Lee
                                
                                et al.
                            
                            (2011). 
                            Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. 
                            Nature Genetics
                            , 43
                            (6)
                            , 585-589.
                            https://doi.org/10.1038/ng.835
                        

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DOI: 10.1038/ng.835