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收藏Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis
He, Hailan; Cao, Xiaoshuang; He, Fang; Zhang, Wen; Wang, Xiaole; Peng, Pan; Xie, Changning; Yin, Fei; Li, Dengfeng; Li, Jiada; Wang, Minghui; Kluessendorf, Malte; Jentsch, Thomas J.; Stauber, Tobias; Peng, Jing
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收藏HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanism
He, Na; Guan, Bao-Zhu; Wang, Jie; Liu, Han-Kui; Mao, Yong; Liu, Zhi-Gang; Yin, Fei; Peng, Jing; Xiao, Bo; Tang, Bei-sha; Zhou, Dong; Huang, Guang; Dai, Qi-Lin; Zeng, Ying; Han, Hong; Zhai, Qiong-Xiang; Li, Bin; Tang, Bin; Li, Wen-Bin; Song, Wang; Liu, Liu; Shi, Yi-Wu; Li, Bing-Mei; Su, Tao; Zhou, Peng; Liu, Xiao-Rong; Guo, Li-Wu; Yi, Yong-Hong; Liao, Wei-Ping
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收藏Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment
Liu, Fang; Liang, Chen; Li, Zhengchang; Zhao, Sen; Yuan, Haiming; Yao, Ruen; Qin, Zailong; Shangguan, Shaofang; Zhang, Shujie; Zou, Li-Ping; Chen, Qian; Gao, Zhijie; Wen, Suiwen; Peng, Jing; Yin, Fei; Chen, Fei; Qiu, Xiaoxia; Luo, Jingsi; Xie, Yingjun; Lu, Dian; Zhang, Yu; Xie, Hua; Li, Guozhuang; Zhang, Terry Jianguo; Luan, Pengfei; Wang, Hongying; Cui, Xiaodai; Huang, Hailiang; Liu, Ruize; Sun, Xiaofang; Chen, Chao; Wu, Nan; Wang, Jian; Liu, Chunyu; Shen, Yiping; Gusella, James F.; Chen, Xiaoli
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