Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes

Friederike Ehrhart*, Susan Steinbusch - Coort, Elisa Cirillo, Eric Smeets, Chris T. Evelo, Leopold M. G. Curfs

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Article number158
Number of pages13
JournalOrphanet Journal of Rare Diseases
Volume11
DOIs
Publication statusPublished - 25 Nov 2016

Keywords

  • Bioinformatics
  • DNA methylation
  • Data integration
  • Epigenetics
  • MECP2
  • Rett syndrome
  • Systems biology
  • DEPENDENT PHOSPHORYLATION
  • AUTISM
  • DNA METHYLATION
  • CPG-BINDING PROTEIN-2
  • TRANSCRIPTIONAL REPRESSOR MECP2
  • BDNF TRANSCRIPTION
  • MOUSE MODEL
  • BIOGENIC-AMINES
  • GENE-EXPRESSION
  • BRAIN

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