Increased level of RAB39B leads to neuronal dysfunction and behavioural changes in mice

Duplications of the Xq28 region are a common cause of X‐linked intellectual disability (XLID). The RAB39B gene locates in Xq28 and has been implicated in disease pathogenesis. However, whether increased dosage of RAB39B leads to cognitive impairment and synaptic dysfunction remains elusive. Herein,...

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Detalles Bibliográficos
Autores principales: Wang, Zijie, Niu, Mengxi, Zheng, Naizhen, Meng, Jian, Jiang, Yiru, Yang, Dingting, Yao, Peijie, Yao, Tingting, Luo, Hong, Xu, Huaxi, Ge, Yunlong, Zhang, Yun‐wu, Zhang, Xian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148058/
https://www.ncbi.nlm.nih.gov/pubmed/36977207
http://dx.doi.org/10.1111/jcmm.17704

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148058/
https://www.ncbi.nlm.nih.gov/pubmed/36977207
http://dx.doi.org/10.1111/jcmm.17704

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