13229_2018_247_MOESM10_ESM.pdf (896.58 kB)
Additional file 10: of Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model
journal contribution
posted on 2018-12-13, 05:00 authored by Hui Guo, Tianyun Wang, Huidan Wu, Min Long, Bradley Coe, Honghui Li, Guanglei Xun, Jianjun Ou, Biyuan Chen, Guiqin Duan, Ting Bai, Ningxia Zhao, Yidong Shen, Yun Li, Yazhe Wang, Yu Zhang, Carl Baker, Yanling Liu, Nan Pang, Lian Huang, Lin Han, Xiangbin Jia, Cenying Liu, Hailun Ni, Xinyi Yang, Lu Xia, Jingjing Chen, Lu Shen, Ying Li, Rongjuan Zhao, Wenjing Zhao, Jing Peng, Qian Pan, Zhigao Long, Wei Su, Jieqiong Tan, Xiaogang Du, Xiaoyan Ke, Meiling Yao, Zhengmao Hu, Xiaobing Zou, Jingping Zhao, Raphael Bernier, Evan Eichler, Kun XiaFigure S6. Distribution of mutations in some of the top mutated genes (DYRK1A, ASXL3, WDFY3 and MECP2) in the ACGC cohort (above) compared to previously published LGD and missense DNMs identified in the SSC and ASC cohorts. (PDF 896 kb)
