Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

J Feldmann, F Le Deist… - British journal of …, 2002 - Wiley Online Library
Familial haemophagocytic lymphohistiocytosis (FHL), an inherited form of haemophagocytic
lymphohistiocytosis (HLH) syndrome, is characterized by the overwhelming activation of T …
被引用次数：170 相关文章
[PDF] academia.edu

[PDF][PDF] Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

J Feldmann, F Le Deist… - British Journal of …, 2002 - academia.edu
Familial haemophagocytic lymphohistiocytosis (FHL), an inherited form of haemophagocytic
lymphohistiocytosis (HLH) syndrome, is characterized by the overwhelming activation of T …

[引用][C] Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

J FELDMANN, F LE DEIST, A FISCHER… - British journal of …, 2002 - pascal-francis.inist.fr
Functional consequences of perforin gene mutations in 22 patients with familial
haemophagocytic lymphohistiocytosis CNRS Inist Pascal-Francis CNRS Pascal and …

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis.

J Feldmann, F Le Deist… - British Journal of …, 2002 - search.ebscohost.com
Familial haemophagocytic lymphohistiocytosis (FHL), an inherited form of haemophagocytic
lymphohistiocytosis (HLH) syndrome, is characterized by the overwhelming activation of T …

[引用][C] Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

J Feldmann, F Le Deist, M Ouachée-Chardin… - British Journal of …, 2002 - cir.nii.ac.jp
Functional consequences of perforin gene mutations in 22 patients with familial
haemophagocytic lymphohistiocytosis | CiNii Research CiNii 国立情報学研究所 学術情報 …

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

J Feldmann, F Le Deist… - British journal of …, 2002 - pubmed.ncbi.nlm.nih.gov
Familial haemophagocytic lymphohistiocytosis (FHL), an inherited form of haemophagocytic
lymphohistiocytosis (HLH) syndrome, is characterized by the overwhelming activation of T …

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis.

J Feldmann, F Le Deist… - British Journal of …, 2002 - europepmc.org
Familial haemophagocytic lymphohistiocytosis (FHL), an inherited form of haemophagocytic
lymphohistiocytosis (HLH) syndrome, is characterized by the overwhelming activation of T …
[PDF] academia.edu

[PDF][PDF] Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

J Feldmann, F Le Deist… - British Journal of …, 2002 - academia.edu
Familial haemophagocytic lymphohistiocytosis (FHL), an inherited form of haemophagocytic
lymphohistiocytosis (HLH) syndrome, is characterized by the overwhelming activation of T …

[引用][C] Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

J FELDMANN, F LE DEIST… - British journal of …, 2002 - Blackwell