A new cohort of MECP2 mutation screening in unexplained mental retardation: careful re-evaluation is the best indicator for molecular diagnosis

Am J Med Genet A. 2006 Jul 15;140(14):1603-7. doi: 10.1002/ajmg.a.31314.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cohort Studies
  • DNA / genetics
  • Female
  • Genetic Testing
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Methyl-CpG-Binding Protein 2 / genetics*
  • Mutation*
  • Phenotype
  • Rett Syndrome / genetics

Substances

  • MECP2 protein, human
  • Methyl-CpG-Binding Protein 2
  • DNA