TEP1 is a risk gene for sporadic cerebral palsy

doi: 10.1016/j.jgg.2021.08.010

• Yangong Wang ¹ , 
• Yiran Xu ^2,3 , 
• Hongwei Li ² , 
• Tianxiang Tang ⁴ , 
• Yimeng Qiao ¹ , 
• Ye Cheng ¹ , 
• Lingling Zhang ² , 
• Juan Song ² , 
• Yu Su ¹ , 
• Xiaoli Zhang ² , 
• Jun Wang ² , 
• Qing Shang ⁵ , 
• Lili Song ¹ , 
• Chao Gao ⁵ , 
• Dengna Zhu ² , 
• Xiaoyang Wang ^2,6 , 
• Changlian Zhu ^2,7,8     , 
• Qinghe Xing ^1,9    

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  1. Institutes of Biomedical Sciences and Children's Hospital, Fudan University, Shanghai 201102, China;

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  2. Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, Department of Pediatrics, The 3rd Affiliated Hospital of Zhengzhou University and Institute of Neuroscience, Zhengzhou 450052, China;

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  3. Commission Key Laboratory of Birth Defects Prevention, Henan Key Laboratory of Population Defects Prevention, Zhengzhou 450052, China;

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  4. Institutes of Brain Science, State Key Laboratory of Medical Neurobiology and Collaborative Innovation Center for Brain Science, Fudan University, Shanghai 200032, China;

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  5. Department of Pediatrics, Children's Hospital of Zhengzhou University and Henan Children's Hospital, Zhengzhou 450053, China;

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  6. Centre of Perinatal Medicine and Health, Sahlgrenska Academy, University of Gothenburg, Gothenburg 40530, Sweden;

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  7. Department of Women's and Children's Health, Karolinska Institutet, Stockholm 17177, Sweden;

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  8. Center for Brain Repair and Rehabilitation, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg 40530, Sweden;

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  9. Shanghai Center for Women and Children's Health, Shanghai 200062, China