Guo, Hui Wang, Tianyun Wu, Huidan Long, Min Coe, Bradley Li, Honghui Xun, Guanglei Ou, Jianjun Chen, Biyuan Duan, Guiqin Bai, Ting Zhao, Ningxia Shen, Yidong Li, Yun Wang, Yazhe Zhang, Yu Baker, Carl Liu, Yanling Pang, Nan Huang, Lian Han, Lin Jia, Xiangbin Liu, Cenying Ni, Hailun Yang, Xinyi Xia, Lu Chen, Jingjing Shen, Lu Li, Ying Zhao, Rongjuan Zhao, Wenjing Peng, Jing Pan, Qian Long, Zhigao Su, Wei Tan, Jieqiong Du, Xiaogang Ke, Xiaoyan Yao, Meiling Hu, Zhengmao Zou, Xiaobing Zhao, Jingping Bernier, Raphael Eichler, Evan Xia, Kun Additional file 10: of Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model Figure 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) Autism spectrum disorders;Targeted sequencing;De novo mutations;Multiple hit;Multifactorial model;Genotype–phenotype relationship 2018-12-13
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