Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain

Lignende værker

• Functional characterisation of MeCP2 mutations found in male patients with X linked mental retardation
  af: Kudo, S, et al.
  Udgivet: (2002)
• Structural basis of MeCP2 distribution on non-CpG methylated and hydroxymethylated DNA
  af: Sperlazza, M. Jeannette, et al.
  Udgivet: (2017)
• Methyl-CpG-Binding Protein MeCP2 Represses Sp1-Activated Transcription of the Human Leukosialin Gene When the Promoter Is Methylated
  af: Kudo, Shinichi
  Udgivet: (1998)
• Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2.
  af: Nan, X, et al.
  Udgivet: (1993)
• MeCP2: Making sense of missense in Rett syndrome
  af: Banerjee, Abhishek, et al.
  Udgivet: (2013)