Rett syndrome linked to defects in forming the MeCP2/Rbfox/LASR complex in mouse models

Rett syndrome (RTT) is a severe neurological disorder and a leading cause of intellectual disability in young females. RTT is mainly caused by mutations found in the X-linked gene encoding methyl-CpG binding protein 2 (MeCP2). Despite extensive studies, the molecular mechanism underlying RTT pathoge...

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Detalles Bibliográficos
Autores principales: Jiang, Yan, Fu, Xing, Zhang, Yuhan, Wang, Shen-Fei, Zhu, Hong, Wang, Wei-Kang, Zhang, Lin, Wu, Ping, Wong, Catherine C. L., Li, Jinsong, Ma, Jinbiao, Guan, Ji-Song, Huang, Ying, Hui, Jingyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486766/
https://www.ncbi.nlm.nih.gov/pubmed/34599184
http://dx.doi.org/10.1038/s41467-021-26084-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486766/
https://www.ncbi.nlm.nih.gov/pubmed/34599184
http://dx.doi.org/10.1038/s41467-021-26084-3

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