Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome

Lignende værker

• Rett Syndrome and MeCP2
  af: Liyanage, Vichithra R. B., et al.
  Udgivet: (2014)
• Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots
  af: Wan, Mimi, et al.
  Udgivet: (1999)
• Complexities of Rett Syndrome and MeCP2
  af: Samaco, Rodney C., et al.
  Udgivet: (2011)
• Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease
  af: Pejhan, Shervin, et al.
  Udgivet: (2021)
• Mutational Analysis of Methyl‐CpG Binding Protein 2 (MECP2) Gene in Indian Cases of Rett Syndrome
  af: Das, Dhanjit Kumar, et al.
  Udgivet: (2013)