Associated Papers
The opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunity.
Mansour R et al.
The Journal of Allergy and Clinical Immunology, 2023
FHLdb: A Comprehensive Database on the Molecular Basis of Familial Hemophagocytic Lymphohistiocytosis.
Viñas-Giménez L et al.
Frontiers in Immunology, 2020
32076423 (PubMed )
Supplement: Table_1.XLSX › Supplementary_Table_1
Multiple inherited sequence variations in two disease-causing genes in familial haemophagocytic lymphohistiocytosis.
Rudd E et al.
British Journal of Haematology, 2009
Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies.
Rudd E et al.
Journal of Medical Genetics, 2006
Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11.
zur Stadt U et al.
Human Molecular Genetics, 2005
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