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Misregulation of Alternative Splicing in a Mouse Model of Rett Syndrome
Mutations in the human MECP2 gene cause Rett syndrome (RTT), a severe neurodevelopmental disorder that predominantly affects girls. Despite decades of work, the molecular function of MeCP2 is not fully understood. Here we report a systematic identification of MeCP2-interacting proteins in the mouse...
Autores principales: | Li, Ronghui, Dong, Qiping, Yuan, Xinni, Zeng, Xin, Gao, Yu, Chiao, Cassandra, Li, Hongda, Zhao, Xinyu, Keles, Sunduz, Wang, Zefeng, Chang, Qiang |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924826/ https://www.ncbi.nlm.nih.gov/pubmed/27352031 http://dx.doi.org/10.1371/journal.pgen.1006129 |
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