Identification of anSH2D1A mutation in a hypogammaglobulinemic male patient with a diagnosis of common variable immunodeficiency

This publication has 26 references indexed in Scilit:

• Hematologic complications of primary immune deficiencies
  Blood 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 patients
  Human Genetics, 1999
• Common Variable Immunodeficiency: Clinical and Immunological Features of 248 Patients
  Clinical 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 Discovery
  Pediatric 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 report
  The Journal of Pediatrics, 1980
• X-LINKED RECESSIVE PROGRESSIVE COMBINED VARIABLE IMMUNODEFICIENCY (DUNCAN'S DISEASE)
  The Lancet, 1975