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...
| Main Authors: | , , , , , , , , , , |
|---|---|
| Format: | Article |
| Jezik: | English |
| Izdano: |
Public Library of Science (PLoS)
2016-06-01
|
| Serija: | PLoS Genetics |
| Online dostop: | http://europepmc.org/articles/PMC4924826?pdf=render |