Novel mutation of the perforin gene and maternal uniparental disomy 10 in a patient with familial hemophagocytic lymphohistiocytosis. [electronic resource]

By: Contributor(s): Producer: 20081014Description: 621-4 p. digitalISSN:
  • 1536-3678
Subject(s): Online resources: In: Journal of pediatric hematology/oncology vol. 30
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Publication Type: Case Reports; Journal Article

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