Developmental arrest of astrocyte lineage in Snai2 deletion mice: implication for the intellectual disability in patients with Waardenburg syndrome

Abstract This study aimed to explore the neurobiological mechanism underlying intellectual disability (ID) in patients with Waardenburg syndrome (WS) identified in a Chinese family. The proband was initially diagnosed with severe ID and then 10 of the 11 extended family members underwent further med...

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Detalhes bibliográficos

Principais autores:	Chaobiao Xue, Haiyun Xu, Xiuyuan Huang, Miaotong Su, Lifang He, Guangping Zhang, Zhexuan Lin, Hui Li, Xiaohong Hong, Shaoxian Chen, Zhuozhi Dai, Tongtong Cai, Can Chen, Yun Lin, Guohong Zhang, Wenhong Luo
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Nature Publishing Group 2025-10-01
Colecção:	Translational Psychiatry
Acesso em linha:	https://doi.org/10.1038/s41398-025-03616-9
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