Current developments in the genetics of Rett and Rett-like syndrome

Friederike Ehrhart, Nasim B. Sangani, Leopold M. G. Curfs

Research output: Contribution to journalReview articleAcademicpeer-review

Original languageEnglish
Pages (from-to)103-108
Number of pages6
JournalCurrent Opinion in Psychiatry
Volume31
Issue number2
DOIs
Publication statusPublished - 1 Mar 2018

Keywords

  • clinical phenotype
  • Mendelian disorder
  • rare disorder
  • whole exome sequencing
  • SEVERE INTELLECTUAL DISABILITY
  • MUTATIONS
  • MECP2
  • PHENOTYPES
  • EXOME
  • VARIANTS
  • DISEASE
  • PATIENT
  • RETARDATION
  • DISORDERS

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