The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited missense mutations in the perforin (PFN1) gene

• VOSKOBOINIK I

収録刊行物

• J Exp Med

  J Exp Med 200 811-816, 2004

詳細情報

• CRID: 1570009749229223808
• NII論文ID: 30017434140
• DOI: 10.1084/jem.20040776
• データソース種別:
  • CiNii Articles