KCC2 rescues functional deficits in human neurons derived from patients with Rett syndrome

Rett syndrome is a severe form of autism spectrum disorder, mainly caused by mutations of a single gene methyl CpG binding protein 2 (MeCP2) on the X chromosome. Patients with Rett syndrome exhibit a period of normal development followed by regression of brain function and the emergence of autistic...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Proc Natl Acad Sci U S A
Egile Nagusiak: Tang, Xin, Kim, Julie, Zhou, Li, Wengert, Eric, Zhang, Lei, Wu, Zheng, Carromeu, Cassiano, Muotri, Alysson R., Marchetto, Maria C. N., Gage, Fred H., Chen, Gong
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: National Academy of Sciences 2016
Gaiak:
Biological Sciences
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4725523/
https://ncbi.nlm.nih.gov/pubmed/26733678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1524013113
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