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...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής

Κύριοι συγγραφείς:	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
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	Nature Publishing Group 2025-10-01
Σειρά:	Translational Psychiatry
Διαθέσιμο Online:	https://doi.org/10.1038/s41398-025-03616-9
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