Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome

2q23.1 microdeletion syndrome is characterized by intellectual disability, motor delay, autistic-like behaviors, and a distinctive craniofacial phenotype. All patients carry a partial or total deletion of methyl-CpG-binding domain protein 5 (MBD5), suggesting that haploinsufficiency of this gene is...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Camarena, Vladimir, Cao, Lei, Abad, Clemer, Abrams, Alexander, Toledo, Yaima, Araki, Kimi, Araki, Masatake, Walz, Katherina, Young, Juan I
Format: Artigo
Sprog:Inglês
Udgivet: BlackWell Publishing Ltd 2014
Fag:
Research Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4154129/
https://ncbi.nlm.nih.gov/pubmed/25001218
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/emmm.201404044
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker