Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett Syndrome

Hum Genet. 2010 Jan;127(1):117.
No abstract available

MeSH terms

  • Base Sequence
  • Codon / genetics
  • Frameshift Mutation
  • Humans
  • India
  • Methyl-CpG-Binding Protein 2 / genetics*
  • Molecular Sequence Data
  • Mutagenesis, Insertional*
  • Rett Syndrome / genetics*
  • Sequence Analysis, DNA

Substances

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

Associated data

  • GENBANK/FJ212168