Large deletions of the MECP2 gene in Chinese patients with classical Rett syndrome

Clin Genet. 2006 Nov;70(5):418-9. doi: 10.1111/j.1399-0004.2006.00694.x.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Asian Continental Ancestry Group / genetics
  • Child
  • Child, Preschool
  • China
  • Exons
  • Female
  • Humans
  • Methyl-CpG-Binding Protein 2 / genetics*
  • Nucleic Acid Amplification Techniques
  • Rett Syndrome / genetics*
  • Sequence Deletion*
  • X Chromosome Inactivation

Substances

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