Author Correction: The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome

Lignende værker

• Mutation analysis of the MECP2 gene in Romanian females with Rett syndrome
  af: Dumitriu Simona, et al.
  Udgivet: (2013-12-01)
• Rett Syndrome without MECP2 Mutation in a Pakistani Girl
  af: Rubina Dad, et al.
  Udgivet: (2020-04-01)
• Rett Syndrome and the Role of MECP2: Signaling to Clinical Trials
  af: Adele Gaspar Lopes, et al.
  Udgivet: (2024-01-01)
• Identification of molecular signatures and pathways involved in Rett syndrome using a multi-omics approach
  af: Ainhoa Pascual-Alonso, et al.
  Udgivet: (2023-09-01)
• Progressive Encephalopathy in Boys with Symptoms of Rett Syndrome and MECP2 Mutations
  af: J Gordon Millichap
  Udgivet: (2006-08-01)