Human iPSC-derived neuron of 16p11.2 deletion reveals haplotype-specific expression of <i>MAPK3</i> and its contribution to variable NDD phenotypes
Fang Liu(Capital Institute of Pediatrics), Xiaoli Chen(Hebei Medical University), Ruize Liu(Xi'an University of Architecture and Technology), Haiming Yuan(Dongguan People’s Hospital), Hailiang Huang(Yantai University), Zhengchang Li(Capital Institute of Pediatrics), Yingjun Xie(Third Affiliated Hospital of Guangzhou Medical University), Nan Wu(Chongqing University), James F. Gusella(Broad Institute), Li‐Ping Zou(Public Health Clinical Center of Chengdu), Yiping Shen(Zhejiang Chinese Medical University), Sen Zhao(University of Oslo), Jing Peng(Central South University), Ruen Yao(Shanghai Jiao Tong University), Suiwen Wen(Guangzhou Medical University), Jinsi Luo(Guangxi Maternal and Child Health Hospital), Xiaodai Cui(Capital Institute of Pediatrics), Fei Yin(Central South University), Zailong Qin(Guangxi Maternal and Child Health Hospital), Chunyu Liu(Central South University), Jian Wang(Shanghai Jiao Tong University), Fei Chen(Guangxi Maternal and Child Health Hospital), Chao Chen(Jiangsu University), Qian Chen(Capital Institute of Pediatrics), Yu Zhang(Wannan Medical College), Xiaofang Sun(Third Affiliated Hospital of Guangzhou Medical University), Dian Lu(Third Affiliated Hospital of Guangzhou Medical University), Shujie Zhang(Northeast Normal University), Xiaoxia Qiu(Fujian Medical University), Liang Chen(Chinese Academy of Medical Sciences & Peking Union Medical College), Hongying Wang(Soochow University), Zhijie Gao(Capital Institute of Pediatrics), Shaofang Shangguan(Capital Institute of Pediatrics), Hua Xie(Capital Institute of Pediatrics)
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