Clinical Study of 8 Cases of CHD2 Gene Mutation–Related Neurological Diseases and Their Mechanisms

Background: The chromodomain helicase DNA-binding protein 2 (CHD2) gene, is an ATPase and part of the CHD family of chromatin remodelers. Mutations in the CHD2 gene are inherited in an autosomal-dominant manner and can lead to intellectual disability, epilepsy, and autism. We investigated the clinic...

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Detalles Bibliográficos
Autores principales: Luo, Xiaona, Sun, Xiaoang, Wang, Yilin, Lin, Longlong, Yuan, Fang, Wang, Simei, Zhang, Wenjing, Ji, Xiaobing, Liu, Meiyan, Wu, Shengnan, Lan, Xiaoping, Zhang, Jie, Yan, Jingbin, Zeng, Fanyi, Chen, Yucai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977407/
https://www.ncbi.nlm.nih.gov/pubmed/35386198
http://dx.doi.org/10.3389/fcell.2022.853127

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