RAB39B Deficiency Impairs Learning and Memory Partially Through Compromising Autophagy

RAB39B is located on the X chromosome and encodes the RAB39B protein that belongs to the RAB family. Mutations in RAB39B are known to be associated with X-linked intellectual disability (XLID), Parkinson’s disease, and autism. However, the patho/physiological functions of RAB39B remain largely unkno...

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Detalles Bibliográficos
Autores principales: Niu, Mengxi, Zheng, Naizhen, Wang, Zijie, Gao, Yue, Luo, Xianghua, Chen, Zhicai, Fu, Xing, Wang, Yanyan, Wang, Ting, Liu, Manqing, Yao, Tingting, Yao, Peijie, Meng, Jian, Zhou, Yunqiang, Ge, Yunlong, Wang, Zhanxiang, Ma, Qilin, Xu, Huaxi, Zhang, Yun-wu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753041/
https://www.ncbi.nlm.nih.gov/pubmed/33364235
http://dx.doi.org/10.3389/fcell.2020.598622

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