Loading...

Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2

Rett syndrome (RTT) is a postnatal neurodevelopmental disorder characterized by the loss of acquired motor and language skills, autistic features, and unusual stereotyped movements. RTT is caused by mutations in the X-linked gene encoding methyl-CpG binding protein 2 (MeCP2). Mutations in MECP2 caus...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Young, Juan I., Hong, Eugene P., Castle, John C., Crespo-Barreto, Juan, Bowman, Aaron B., Rose, Matthew F., Kang, Dongcheul, Richman, Ron, Johnson, Jason M., Berget, Susan, Zoghbi, Huda Y.
Format: Artigo
Sprog:Inglês
Udgivet: National Academy of Sciences 2005
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1266160/
https://ncbi.nlm.nih.gov/pubmed/16251272
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0507856102
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!