MECP2 mutations account for most cases of typical forms of Rett syndrome

• BIENVENU T

収録刊行物

• Hum Mol Genet

  Hum Mol Genet 9 1377-1384, 2000

詳細情報

• CRID: 1571417125628248576
• NII論文ID: 30018401393
• DOI: 10.1093/hmg/9.9.1377
• データソース種別:
  • CiNii Articles