Author:
Luo Xiaoqing,Li Cheng,Wang Xiaolu,Yu Xiaoli,Jiang Jun
Funder
the project of Wuhan Municipal Health Planning Commission
Nature Science Foundation of Hubei Province
Wuhan clinical medical research in children’s neural disease
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Medicine
Reference13 articles.
1. Migeon BR, Dunn MA, Thomas G, Schmeckpeper BJ, Naidu S. Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome. Am J Hum Genet. 1995;56(3):647–53.
2. Neurobiology WAE. Domains to the rescue for Rett syndrome. Nature. 2017;550(7676):343–4.
3. Stancheva I, Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR. A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos. Mol Cell. 2003;12(2):425–35.
4. Yang Y, Kucukkal TG, Li J, Alexov E, Cao W. Binding Analysis of Methyl-CpG Binding Domain of MeCP2 and Rett Syndrome Mutations. ACS Chem Biol. 2016;21(11(10)):2706–15.
5. Guerrini R, Parrini E. Epilepsy in Rett syndrome, and CDKL5- and FOXG1-gene-related encephalopathies. Epilepsia. 2012;53(12):2067–78.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献