TEP1 is a risk gene for sporadic cerebral palsy

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作   者：

Yangong Wang;  Yiran Xu;  Hongwei Li;  Tianxiang Tang;  Yimeng Qiao;  Ye Cheng;  Lingling Zhang;  Juan Song;  Yu Su;  Xiaoli Zhang;  Jun Wang;  Qing Shang;  Lili Song;  Chao Gao;  Dengna Zhu;  Xiaoyang Wang;  Changlian Zhu;  Qinghe Xing; 

作者机构：

Department of Pediatrics;  Institutes of Brain Science;  Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center;  Institutes of Biomedical Sciences and Children's Hospital; 

期刊名称：

Journal of Genetics and Genomics

i s s n：

1673-8527

年卷期：

2021 年 012 期

页   码：

1134-1138

摘   要：

Cerebral palsy （CP） is a nonprogressive dyskinesia syndrome caused by early brain injury,with an incidence of approximately2.0—3.5/1000 live births worldwide （Li et al.,2021;Moreno-DeLuca et al.,2021）.Currently,there are more than 300,000 children aged 0—6 years diagnosed with CP in China （Liu et al.,1999;Yang et al.,2021）,thus making it one of the most common debilitating diseases affecting children.