X-linked lymphoproliferative disease: Genetic lesions and clinical consequences
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pulmonary and Respiratory Medicine,Immunology and Allergy,Immunology
Link
http://link.springer.com/content/pdf/10.1007/s11882-002-0068-0.pdf
Reference49 articles.
1. Purtilo DT, Cassel CK, Yang JP, Harper R: X-linked recessive progressive combined variable immunodeficiency (Duncan’s disease). Lancet 1975, 1:935–940.
2. Seemayer TA, Gross TG, Egeler RM, et al.: X-linked lymphoproliferative disease: twenty-five years after the discovery. Pediatr Res 1995, 38:471–478.
3. Hamilton JK, Paquin LA, Sullivan JL, et al.: X-linked lymphoproliferative syndrome registry report. J Pediatr 1980, 96:669–673.
4. Seemayer TA, Grierson H, Pirruccello SJ, et al.: X-linked lymphoproliferative disease. Am J Dis Child 1993, 147:1242–1245.
5. Morra M, Silander O, Calpe S, et al.: Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome. Blood 2001, 98:1321–1325. Reports on six patients diagnosed with common variable immunodeficiency subsequently found to have mutations in the SAP gene. Four of six died of infection or complications of infections.
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