Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis
✍ Scribed by Stepp, Susan E. (author);Dufourcq-Lagelouse, Rémi (author);Le Deist, Françoise (author);Bhawan, Sadhna (author);Certain, Stéphanie (author);Mathew, Porunelloor A. (author);Henter, Jan Inge (author);Bennett, Michael (author);Fischer, Alain (author);De Saint Basile, Geneviève (author);Kumar, Vinay (author)
- Book ID
- 121161871
- Publisher
- American Association for the Advancement of Science
- Year
- 1999
- Tongue
- English
- Weight
- 347 KB
- Volume
- 286
- Category
- Article
- ISSN
- 0036-8075
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📜 SIMILAR VOLUMES
## Abstract Since the discovery of __perforin__ gene mutations in familial hemophagocytic lymphohistiocytosis (FHL) type 2, heterogeneous features in FHL2 patients have been identified in a report of Feldmann et al. as the beginning. This study was conducted to determine the impact of characteristi