De novo mutations revealed by whole-exome sequencing are strongly associated with autism
全外显子组测序揭示的新生突变与自闭症密切相关
期刊:Nature
影响因子:48.5
doi:10.1038/nature10945
Sanders, Stephan J; Murtha, Michael T; Gupta, Abha R; Murdoch, John D; Raubeson, Melanie J; Willsey, A Jeremy; Ercan-Sencicek, A Gulhan; DiLullo, Nicholas M; Parikshak, Neelroop N; Stein, Jason L; Walker, Michael F; Ober, Gordon T; Teran, Nicole A; Song, Youeun; El-Fishawy, Paul; Murtha, Ryan C; Choi, Murim; Overton, John D; Bjornson, Robert D; Carriero, Nicholas J; Meyer, Kyle A; Bilguvar, Kaya; Mane, Shrikant M; Sestan, Nenad; Lifton, Richard P; Günel, Murat; Roeder, Kathryn; Geschwind, Daniel H; Devlin, Bernie; State, Matthew W