An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene

• SETHURAMAN G

収録刊行物

• Clin Exp Dermatol

  Clin Exp Dermatol 30 286-288, 2005

詳細情報

• CRID: 1572824498893555200
• NII論文ID: 30015014449
• DOI: 10.1111/j.1365-2230.2004.01712.x
• データソース種別:
  • CiNii Articles