Identification of anSH2D1A mutation in a hypogammaglobulinemic male patient with a diagnosis of common variable immunodeficiency
- 1 February 2003
- journal article
- case report
- Published by Springer Science and Business Media LLC in International Journal of Hematology
- Vol. 78 (1), 45-47
- https://doi.org/10.1007/bf02983239
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Hematologic complications of primary immune deficienciesBlood Reviews, 2002
- Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2)Cell, 2000
- SH2D1A mutation analysis for diagnosis of XLP in typical and atypical patientsHuman Genetics, 1999
- Common Variable Immunodeficiency: Clinical and Immunological Features of 248 PatientsClinical Immunology, 1999
- Matched unrelated allogeneic bone marrow transplantation for recurrent malignant lymphoma in a patient with X-linked lymphoproliferative disease (XLP)Bone Marrow Transplantation, 1998
- X-Linked Lymphoproliferative Disease: Twenty-Five Years after the DiscoveryPediatric Research, 1995
- Failure in antigen responses by T ceils from patients with common variable immunodeficiency (CVID)Clinical and Experimental Immunology, 1994
- Evaluation of families wherein a single male manifests a phenotype of X‐linked lymphoproliferative disease (XLP)American Journal of Medical Genetics, 1993
- X-Linked Lymphoproliferative Syndrome Registry reportThe Journal of Pediatrics, 1980
- X-LINKED RECESSIVE PROGRESSIVE COMBINED VARIABLE IMMUNODEFICIENCY (DUNCAN'S DISEASE)The Lancet, 1975