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Report of a novel missense mutation in the MECP2 gene in a middle-aged man with intellectual disability syndrome.

Maria ArvioMaria K HaanpääPia PohjolaJaana Lähdetie
Published in: Clinical case reports (2021)
Exome sequencing revealed the cause of our 35-year-old male patient's progressive and severe intellectual and motor disability, namely a previously undescribed missense mutation of MECP2.
Keyphrases
  • intellectual disability
  • middle aged
  • autism spectrum disorder
  • multiple sclerosis
  • case report
  • single cell
  • copy number
  • genome wide