WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype

Lignende værker

• WDR45 Mutation in Atypical Rett Syndrome with Brain Iron Accumulation
  af: Crisp, Sarah J., et al.
  Udgivet: (2015)
• A novel WDR45 mutation in a patient with β-propeller protein-associated neurodegeneration
  af: Wynn, DonRaphael P., et al.
  Udgivet: (2016)
• MECP2 Mutations in People without Rett Syndrome
  af: Suter, Bernhard, et al.
  Udgivet: (2014)
• Spectrum of MECP2 mutations in Vietnamese patients with RETT syndrome
  af: Le Thi Thanh, Huong, et al.
  Udgivet: (2018)
• Structural investigation of Rett-inducing MeCP2 mutations()
  af: Spiga, Ottavia, et al.
  Udgivet: (2018)