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  • Title: IgG subclass levels and southern analysis of DNA in primary immunodeficiency diseases including IgG subclass deficiency.
    Author: Miwa Y, Inoue R, Ozawa T, Kondo N, Orii T.
    Journal: Exp Clin Immunogenet; 1994; 11(4):173-81. PubMed ID: 7857662.
    Abstract:
    Serum IgG subclass levels are reported for twenty patients with primary immunodeficiency diseases, including four patients with IgG subclass deficiency, using an enzyme-linked immunosorbent assay with monoclonal antibodies. The disorder of each patient with IgG subclass deficiency seemed to be heterogeneous immunologically and clinically. One had complete IgG2-IgG4 deficiency, another had IgG2-IgG4-IgA deficiency and the other two had IgG2-IgA deficiencies. We did not find any structural-gene deletions in the constant region of the human immunoglobulin heavy-chain locus. Although the possibility of defects in genes controlling immunoglobulin expression, or small mutations, remains, these results suggest that IgG subclass deficiency is not always linked to particular structural-gene deletions.
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