Art
J-GLOBAL ID：200902282996635837
Reference number：03A0517760
Identification of an SH2D1A Mutation in a Hypogammaglobulinemic Male Patient with a Diagnosis of Common Variable Inununodeficiency
通常の各種免疫不全症と診断された低ガンマグロブリン血症男性患者におけるSH2D1A遺伝子変異の同定
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Material：
Volume：
78
Issue：
1
Page：
45-47
Publication year：
Jul. 2003
JST Material Number：
F0888A
ISSN：
0925-5710
CODEN：
IJHEEY
Document type：
Article
Article type：
原著論文
Country of issue：
Germany, Federal Republic of (DEU)
Language：
ENGLISH (EN)
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JST classification (2)：
JST classification
Category name(code) classified by JST.
Hematologic diagnosis
, Diagnostics of immunologic diseases,allergic diseases.
Reference (26)：
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CUNNINGHAM-RUNDLES, C. Common variable immunodeficiency : clinical and immunological features of 248 patients. Clin Immunol. 1999, 92, 34-48
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CUNNINGHAM-RUNDLES, C. Hematologic complications of primary immune deficiencies. Blood Rev. 2002, 16, 61-64
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SPICKETT, GP. Cellular abnormalities in common variable immunodeficiency. Immunodefic Rev. 1990, 2, 199-219
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STAGG, AJ. Failure in antigen responses by T cells from patients with common variable immunodeficiency (CVID). Clin Exp Immunol. 1994, 96, 48-53
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FISCHER, MB. A defect in the early phase of T-cell receptor-mediated T-cell activation in patients with common variable immunodeficiency. Blood. 1994, 84, 4234-4241
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