Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

J Med Genet. 2000 Dec;37(12):E41. doi: 10.1136/jmg.37.12.e41.
No abstract available

Publication types

  • Letter

MeSH terms

  • Amino Acid Sequence
  • Asian Continental Ancestry Group / genetics
  • Autistic Disorder / genetics*
  • Base Sequence
  • Child, Preschool
  • Chromosomal Proteins, Non-Histone*
  • Codon, Nonsense*
  • DNA Mutational Analysis
  • DNA-Binding Proteins / genetics*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Methyl-CpG-Binding Protein 2
  • Molecular Sequence Data
  • Mutation, Missense*
  • Repressor Proteins / genetics*
  • Rett Syndrome / genetics*

Substances

  • Chromosomal Proteins, Non-Histone
  • Codon, Nonsense
  • DNA-Binding Proteins
  • MECP2 protein, human
  • Methyl-CpG-Binding Protein 2
  • Repressor Proteins