-
1
-
-
0242417491
-
Viral infection results in massive CD8+ T-cell expansion and mortality in vaccinated perforin-deficient mice
-
Badovinac VP, Hamilton SE, Harty JT. Viral infection results in massive CD8+ T-cell expansion and mortality in vaccinated perforin-deficient mice. Immunity 2003 18 463-474
-
(2003)
Immunity
, vol.18
, pp. 463-474
-
-
Badovinac, V.P.1
Hamilton, S.E.2
Harty, J.T.3
-
2
-
-
15844397403
-
Identification of the homologous beige and Chediak-Higashi syndrome genes
-
Barbosa MD, Nguyen QA, Tchernev VT, etal. Identification of the homologous beige and Chediak-Higashi syndrome genes. Nature 1996 382 262-265
-
(1996)
Nature
, vol.382
, pp. 262-265
-
-
Barbosa, M.D.1
Nguyen, Q.A.2
Tchernev, V.T.3
-
3
-
-
34248666067
-
Occult macrophage activation syndrome in patients with systemic juvenile idiopathic arthritis
-
Behrens EM, Beukelman T, Paessler M, etal. Occult macrophage activation syndrome in patients with systemic juvenile idiopathic arthritis. J Rheumatol 2007 34 1133-1138
-
(2007)
J Rheumatol
, vol.34
, pp. 1133-1138
-
-
Behrens, E.M.1
Beukelman, T.2
Paessler, M.3
-
4
-
-
0032101604
-
Aplastic anemia rescued by exhaustion of cytokine-secreting CD8+ T-cells in persistent infection with lymphocytic choriomeningitis virus
-
Binder D, van den Broek MF, Kagi D, etal. Aplastic anemia rescued by exhaustion of cytokine-secreting CD8+ T-cells in persistent infection with lymphocytic choriomeningitis virus. J Exp Med 1998 187 1903-1920
-
(1998)
J Exp Med
, vol.187
, pp. 1903-1920
-
-
Binder, D.1
Van Den Broek, M.F.2
Kagi, D.3
-
6
-
-
34548814973
-
Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients
-
Bryceson YT, Rudd E, Zheng C, etal. Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients. Blood 2007 110 1906-1915
-
(2007)
Blood
, vol.110
, pp. 1906-1915
-
-
Bryceson, Y.T.1
Rudd, E.2
Zheng, C.3
-
7
-
-
34250189190
-
Germline mutations of the perforin gene are a frequent occurrence in childhood anaplastic large cell lymphoma
-
Cannella S, Santoro A, Bruno G, etal. Germline mutations of the perforin gene are a frequent occurrence in childhood anaplastic large cell lymphoma. Cancer 2007 109 2566-2571
-
(2007)
Cancer
, vol.109
, pp. 2566-2571
-
-
Cannella, S.1
Santoro, A.2
Bruno, G.3
-
8
-
-
67649836342
-
Temperature sensitivity of human perforin mutants unmasks subtotal loss of cytotoxicity, delayed FHL, and a predisposition to cancer
-
Chia J, Yeo KP, Whisstock JC, etal. Temperature sensitivity of human perforin mutants unmasks subtotal loss of cytotoxicity, delayed FHL, and a predisposition to cancer. Proc Natl Acad Sci USA 2009 106 9809-9814
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 9809-9814
-
-
Chia, J.1
Yeo, K.P.2
Whisstock, J.C.3
-
9
-
-
21144435788
-
A proportion of patients with lymphoma may harbor mutations of the perforin gene
-
Clementi R, Locatelli F, Dupre L, etal. A proportion of patients with lymphoma may harbor mutations of the perforin gene. Blood 2005 105 4424-4428
-
(2005)
Blood
, vol.105
, pp. 4424-4428
-
-
Clementi, R.1
Locatelli, F.2
Dupre, L.3
-
10
-
-
17344372694
-
Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene
-
Coffey AJ, Brooksbank RA, Brandau O, etal. Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene. Nat Genet 1998 20 129-135
-
(1998)
Nat Genet
, vol.20
, pp. 129-135
-
-
Coffey, A.J.1
Brooksbank, R.A.2
Brandau, O.3
-
11
-
-
72849125357
-
Munc18-2/STXBP2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 (FHL5) and impairs cytotoxic granule exocytosis in patient NK cells
-
in press
-
Côte M, Mnager MM, Burgess A, etal. Munc18-2/STXBP2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 (FHL5) and impairs cytotoxic granule exocytosis in patient NK cells. J Clin Invest 2009 119 in press.
-
(2009)
J Clin Invest
, vol.119
-
-
Côte, M.1
Mnager, M.M.2
Burgess, A.3
-
12
-
-
0035479955
-
The role of cytotoxicity in lymphocyte homeostasis
-
de Saint Basile G, Fischer A. The role of cytotoxicity in lymphocyte homeostasis. Curr Opin Immunol 2001 13 549-554
-
(2001)
Curr Opin Immunol
, vol.13
, pp. 549-554
-
-
De Saint Basile, G.1
Fischer, A.2
-
13
-
-
33745633063
-
Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type II
-
Enders A, Zieger B, Schwarz K, etal. Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type II. Blood 2006 108 81-87
-
(2006)
Blood
, vol.108
, pp. 81-87
-
-
Enders, A.1
Zieger, B.2
Schwarz, K.3
-
14
-
-
10744224641
-
Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3)
-
Feldmann J, Callebaut I, Raposo G, etal. Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3). Cell 2003 115 461-473
-
(2003)
Cell
, vol.115
, pp. 461-473
-
-
Feldmann, J.1
Callebaut, I.2
Raposo, G.3
-
15
-
-
0036277746
-
Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis
-
Feldmann J, Le Deist F, Ouachee-Chardin M, etal. Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis. Br J Haematol 2002 117 965-972
-
(2002)
Br J Haematol
, vol.117
, pp. 965-972
-
-
Feldmann, J.1
Le Deist, F.2
Ouachee-Chardin, M.3
-
16
-
-
0030943203
-
Frequency and severity of central nervous system lesions in hemophagocytic lymphohistiocytosis
-
Haddad E, Sulis ML, Jabado N, etal. Frequency and severity of central nervous system lesions in hemophagocytic lymphohistiocytosis. Blood 1997 89 794-800
-
(1997)
Blood
, vol.89
, pp. 794-800
-
-
Haddad, E.1
Sulis, M.L.2
Jabado, N.3
-
17
-
-
0030937079
-
HLH-94: A treatment protocol for hemophagocytic lymphohistiocytosis. HLH study Group of the Histiocyte Society
-
Henter JI, Arico M, Egeler RM, etal. HLH-94: a treatment protocol for hemophagocytic lymphohistiocytosis. HLH study Group of the Histiocyte Society. Med Pediatr Oncol 1997 28 342-347
-
(1997)
Med Pediatr Oncol
, vol.28
, pp. 342-347
-
-
Henter, J.I.1
Arico, M.2
Egeler, R.M.3
-
18
-
-
0025787766
-
Hypercytokinemia in familial hemophagocytic lymphohistiocytosis
-
Henter JI, Elinder G, Soder O, etal. Hypercytokinemia in familial hemophagocytic lymphohistiocytosis. Blood 1991 78 2918-2922
-
(1991)
Blood
, vol.78
, pp. 2918-2922
-
-
Henter, J.I.1
Elinder, G.2
Soder, O.3
-
19
-
-
0026061971
-
Incidence in Sweden and clinical features of familial hemophagocytic lymphohistiocytosis
-
Henter JI, Elinder G, Soder O, etal. Incidence in Sweden and clinical features of familial hemophagocytic lymphohistiocytosis. Acta Paediatr Scand 1991 80 428-435
-
(1991)
Acta Paediatr Scand
, vol.80
, pp. 428-435
-
-
Henter, J.I.1
Elinder, G.2
Soder, O.3
-
20
-
-
33845619137
-
HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis
-
Henter JI, Horne A, Arico M, etal. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer 2007 48 124-131
-
(2007)
Pediatr Blood Cancer
, vol.48
, pp. 124-131
-
-
Henter, J.I.1
Horne, A.2
Arico, M.3
-
21
-
-
0036786375
-
Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation
-
Henter JI, Samuelsson-Horne A, Arico M, etal. Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation. Blood 2002 100 2367-2373
-
(2002)
Blood
, vol.100
, pp. 2367-2373
-
-
Henter, J.I.1
Samuelsson-Horne, A.2
Arico, M.3
-
22
-
-
20444457982
-
Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis
-
Horne A, Janka G, Maarten Egeler R, etal. Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis. Br J Haematol 2005 129 622-630
-
(2005)
Br J Haematol
, vol.129
, pp. 622-630
-
-
Horne, A.1
Janka, G.2
Maarten Egeler, R.3
-
23
-
-
38349139194
-
Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis
-
Horne A, Trottestam H, Arico M, etal. Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis. Br J Haematol 2008 140 327-335
-
(2008)
Br J Haematol
, vol.140
, pp. 327-335
-
-
Horne, A.1
Trottestam, H.2
Arico, M.3
-
24
-
-
17644442916
-
Treatment of familial hemophagocytic lymphohistiocytosis with bone marrow transplantation from HLA genetically nonidentical donors
-
Jabado N, de Graeff-Meeder ER, Cavazzana-Calvo M, etal. Treatment of familial hemophagocytic lymphohistiocytosis with bone marrow transplantation from HLA genetically nonidentical donors. Blood 1997 90 4743-4748
-
(1997)
Blood
, vol.90
, pp. 4743-4748
-
-
Jabado, N.1
De Graeff-Meeder, E.R.2
Cavazzana-Calvo, M.3
-
25
-
-
77949704386
-
Hemophagocytic lymphohistiocytosis: When the immune system runs amok
-
Janka G. Hemophagocytic lymphohistiocytosis: when the immune system runs amok. Klin Padiatr 2009 221 278-285
-
(2009)
Klin Padiatr
, vol.221
, pp. 278-285
-
-
Janka, G.1
-
26
-
-
3242752040
-
An animal model of hemophagocytic lymphohistiocytosis (HLH): CD8+ T-cells and interferon gamma are essential for the disorder
-
Jordan MB, Hildeman D, Kappler J, etal. An animal model of hemophagocytic lymphohistiocytosis (HLH): CD8+ T-cells and interferon gamma are essential for the disorder. Blood 2004 104 735-743
-
(2004)
Blood
, vol.104
, pp. 735-743
-
-
Jordan, M.B.1
Hildeman, D.2
Kappler, J.3
-
27
-
-
4444330604
-
Case records of the Massachusetts General Hospital, Weekly clinicopathological exercises. Case, 28-2004, Newborn, twins, with thrombocytopenia, coagulation defects, and hepatosplenomegaly
-
Lipton JM, Westra S, Haverty CE, etal. Case records of the Massachusetts General Hospital, Weekly clinicopathological exercises. Case, 28-2004, Newborn, twins, with thrombocytopenia, coagulation defects, and hepatosplenomegaly. N Engl J Med 2004 351 1120-1130
-
(2004)
N Engl J Med
, vol.351
, pp. 1120-1130
-
-
Lipton, J.M.1
Westra, S.2
Haverty, C.E.3
-
28
-
-
34548384442
-
Immunotherapy of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins: A single-center retrospective report of 38 patients
-
Mahlaoui N, Ouachee-Chardin M, de Saint Basile G, etal. Immunotherapy of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins: a single-center retrospective report of 38 patients. Pediatrics 2007 120 e622-e628
-
(2007)
Pediatrics
, vol.120
-
-
Mahlaoui, N.1
Ouachee-Chardin, M.2
De Saint Basile, G.3
-
29
-
-
4043053802
-
Hemophagocytic lymphohistiocytosis presenting with nonimmune hydrops fetalis
-
Malloy CA, Polinski C, Alkan S, etal. Hemophagocytic lymphohistiocytosis presenting with nonimmune hydrops fetalis. J Perinatol 2004 24 458-460
-
(2004)
J Perinatol
, vol.24
, pp. 458-460
-
-
Malloy, C.A.1
Polinski, C.2
Alkan, S.3
-
30
-
-
46749135657
-
Analysis of RAB27A gene in griscelli syndrome type 2: Novel mutations including a deletion hotspot
-
Mamishi S, Modarressi MH, Pourakbari B, etal. Analysis of RAB27A gene in griscelli syndrome type 2: novel mutations including a deletion hotspot. J Clin Immunol 2008 28 384-389
-
(2008)
J Clin Immunol
, vol.28
, pp. 384-389
-
-
Mamishi, S.1
Modarressi, M.H.2
Pourakbari, B.3
-
31
-
-
27744607629
-
Severe imbalance of IL-18/IL-18BP in patients with secondary hemophagocytic syndrome
-
Mazodier K, Marin V, Novick D, etal. Severe imbalance of IL-18/IL-18BP in patients with secondary hemophagocytic syndrome. Blood 2005 106 3483-3489
-
(2005)
Blood
, vol.106
, pp. 3483-3489
-
-
Mazodier, K.1
Marin, V.2
Novick, D.3
-
32
-
-
33747618010
-
Perforin polymorphism A91V and susceptibility to B-precursor childhood acute lymphoblastic leukemia: A report from the Childrens Oncology Group
-
Mehta PA, Davies SM, Kumar A, etal. Perforin polymorphism A91V and susceptibility to B-precursor childhood acute lymphoblastic leukemia: a report from the Childrens Oncology Group. Leukemia 2006 20 1539-1541
-
(2006)
Leukemia
, vol.20
, pp. 1539-1541
-
-
Mehta, P.A.1
Davies, S.M.2
Kumar, A.3
-
33
-
-
34247880547
-
Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4
-
Menager MM, Menasche G, Romao M, etal. Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4. Nat Immunol 2007 8 257-267
-
(2007)
Nat Immunol
, vol.8
, pp. 257-267
-
-
Menager, M.M.1
Menasche, G.2
Romao, M.3
-
35
-
-
0042388106
-
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)
-
Menasche G, Ho CH, Sanal O, etal. Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1). J Clin Invest 2003 112 450-456
-
(2003)
J Clin Invest
, vol.112
, pp. 450-456
-
-
Menasche, G.1
Ho, C.H.2
Sanal, O.3
-
36
-
-
0344002689
-
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
-
Menasche G, Pastural E, Feldmann J, etal. Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome. Nat Genet 2000 25 173-176
-
(2000)
Nat Genet
, vol.25
, pp. 173-176
-
-
Menasche, G.1
Pastural, E.2
Feldmann, J.3
-
37
-
-
12844253028
-
Treatment of primary Epstein-Barr virus infection in patients with X-linked lymphoproliferative disease using B-cell-directed therapy
-
Milone MC, Tsai DE, Hodinka RL, etal. Treatment of primary Epstein-Barr virus infection in patients with X-linked lymphoproliferative disease using B-cell-directed therapy. Blood 2005 105 994-996
-
(2005)
Blood
, vol.105
, pp. 994-996
-
-
Milone, M.C.1
Tsai, D.E.2
Hodinka, R.L.3
-
38
-
-
39749114456
-
Soluble TWEAK is markedly elevated in hemophagocytic lymphohistiocytosis
-
Nagasawa M, Yi Z, Imashuku S, etal. Soluble TWEAK is markedly elevated in hemophagocytic lymphohistiocytosis. Am J Hematol 2008 83 222-225
-
(2008)
Am J Hematol
, vol.83
, pp. 222-225
-
-
Nagasawa, M.1
Yi, Z.2
Imashuku, S.3
-
39
-
-
0030293556
-
Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome
-
Nagle DL, Karim MA, Woolf EA, etal. Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome. Nat Genet 1996 14 307-311
-
(1996)
Nat Genet
, vol.14
, pp. 307-311
-
-
Nagle, D.L.1
Karim, M.A.2
Woolf, E.A.3
-
40
-
-
17744414197
-
Cytokine production regulating Th1 and Th2 cytokines in hemophagocytic lymphohistiocytosis
-
Osugi Y, Hara J, Tagawa S, etal. Cytokine production regulating Th1 and Th2 cytokines in hemophagocytic lymphohistiocytosis. Blood 1997 89 4100-4103
-
(1997)
Blood
, vol.89
, pp. 4100-4103
-
-
Osugi, Y.1
Hara, J.2
Tagawa, S.3
-
41
-
-
70449453484
-
Neutralization of IFN defeats hemophagocytosis in LCMV-infected perforin- and Rab27a-deficient mice
-
in press
-
Pachlopnik Schmid J, Ho CH, Chretien F, etal. Neutralization of IFN defeats hemophagocytosis in LCMV-infected perforin- and Rab27a-deficient mice. EMBO Mol Med in press 2009a
-
(2009)
EMBO Mol Med
-
-
Pachlopnik Schmid, J.1
Ho, C.H.2
Chretien, F.3
-
42
-
-
67651056216
-
Hematopoietic stem cell transplantation in Griscelli syndrome type 2: A single-center report on 10 patients
-
Pachlopnik Schmid J, Moshous D, Boddaert N, etal. Hematopoietic stem cell transplantation in Griscelli syndrome type 2: a single-center report on 10 patients. Blood 2009b 114 211-218
-
(2009)
Blood
, vol.114
, pp. 211-218
-
-
Pachlopnik Schmid, J.1
Moshous, D.2
Boddaert, N.3
-
43
-
-
0034618065
-
X-linked lymphoproliferative disease. 2B4 molecules displaying inhibitory rather than activating function are responsible for the inability of natural killer cells to kill Epstein-Barr virus-infected cells
-
Parolini S, Bottino C, Falco M, etal. X-linked lymphoproliferative disease. 2B4 molecules displaying inhibitory rather than activating function are responsible for the inability of natural killer cells to kill Epstein-Barr virus-infected cells. J Exp Med 2000 192 337-346
-
(2000)
J Exp Med
, vol.192
, pp. 337-346
-
-
Parolini, S.1
Bottino, C.2
Falco, M.3
-
44
-
-
33750597717
-
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
-
Rigaud S, Fondaneche MC, Lambert N. XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome. Nature 2006 444 110-114
-
(2006)
Nature
, vol.444
, pp. 110-114
-
-
Rigaud, S.1
Fondaneche, M.C.2
Lambert, N.3
-
45
-
-
20344362940
-
A single amino acid change A91V in perforin: A novel, frequent predisposing factor to childhood acute lymphoblastic leukemia?
-
Santoro A, Cannella S, Trizzino A, etal. A single amino acid change A91V in perforin: a novel, frequent predisposing factor to childhood acute lymphoblastic leukemia? Haematologica 2005 90 697-698
-
(2005)
Haematologica
, vol.90
, pp. 697-698
-
-
Santoro, A.1
Cannella, S.2
Trizzino, A.3
-
46
-
-
0034605122
-
Perforin-mediated cytotoxicity is critical for surveillance of spontaneous lymphoma
-
Smyth MJ, Thia KY, Street SE, etal. Perforin-mediated cytotoxicity is critical for surveillance of spontaneous lymphoma. J Exp Med 2000 192 755-760
-
(2000)
J Exp Med
, vol.192
, pp. 755-760
-
-
Smyth, M.J.1
Thia, K.Y.2
Street, S.E.3
-
47
-
-
0033520970
-
Perforin gene defects in familial hemophagocytic lymphohistiocytosis
-
Stepp SE, Dufourcq-Lagelouse R, Le Deist F, etal. Perforin gene defects in familial hemophagocytic lymphohistiocytosis. Science 1999 286 1957-1959
-
(1999)
Science
, vol.286
, pp. 1957-1959
-
-
Stepp, S.E.1
Dufourcq-Lagelouse, R.2
Le Deist, F.3
-
49
-
-
0344699322
-
Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance gene
-
Torrents D, Mykkanen J, Pineda M, etal. Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance gene. Nat Genet 1999 21 293-296
-
(1999)
Nat Genet
, vol.21
, pp. 293-296
-
-
Torrents, D.1
Mykkanen, J.2
Pineda, M.3
-
50
-
-
33644669225
-
Correlation between phenotypic heterogeneity and gene mutational characteristics in familial hemophagocytic lymphohistiocytosis (FHL)
-
Ueda I, Ishii E, Morimoto A, etal. Correlation between phenotypic heterogeneity and gene mutational characteristics in familial hemophagocytic lymphohistiocytosis (FHL). Pediatr Blood Cancer 2006 46 482-488
-
(2006)
Pediatr Blood Cancer
, vol.46
, pp. 482-488
-
-
Ueda, I.1
Ishii, E.2
Morimoto, A.3
-
51
-
-
34548038182
-
Perforin activity and immune homeostasis: The common A91V polymorphism in perforin results in both presynaptic and postsynaptic defects in function
-
Voskoboinik I, Sutton VR, Ciccone A, etal. Perforin activity and immune homeostasis: the common A91V polymorphism in perforin results in both presynaptic and postsynaptic defects in function. Blood 2007 110 1184-1190
-
(2007)
Blood
, vol.110
, pp. 1184-1190
-
-
Voskoboinik, I.1
Sutton, V.R.2
Ciccone, A.3
-
52
-
-
70350500464
-
Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11
-
zur Stadt U, Rohr J, Seifert W, etal. Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11. Am J Hum Genet 2009 85 482-492
-
(2009)
Am J Hum Genet
, vol.85
, pp. 482-492
-
-
Zur Stadt, U.1
Rohr, J.2
Seifert, W.3
-
53
-
-
20144363940
-
Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11
-
zur Stadt U, Schmidt S, Kasper B, etal. Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11. Hum Mol Genet 2005 14 827-834
-
(2005)
Hum Mol Genet
, vol.14
, pp. 827-834
-
-
Zur Stadt, U.1
Schmidt, S.2
Kasper, B.3
|