A missense mutation in the coiled-coil motif of the HP1-interacting domain of ATR-X in a family with X-linked mental retardation

Neurogenetics. 2005 Feb;6(1):45-7. doi: 10.1007/s10048-004-0190-3.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Binding Sites
  • Chromosomes, Human, X*
  • Female
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Mutation, Missense*
  • Pedigree
  • Syndrome