Abstract
Hyper-immunoglobulin M (IgM) syndrome (HIGM) is a rare heterogeneous primary immune deficiency. We describe a patient with HIGM characterized by skewed production of serum IgG subclasses and normal somatic hypermutation. This case may represent a subgroup of HIGM type 4 that is characterized by a biased switching to the V-region proximal constant regions.
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CITATION STYLE
McLean, G. R., Miller, K. K., Schrader, J. W., & Junker, A. K. (2004). Biased immunoglobulin G (IgG) subclass production in a case of hyper-IgM syndrome. Clinical and Diagnostic Laboratory Immunology, 11(6), 1192–1193. https://doi.org/10.1128/CDLI.11.6.1192-1193.2004
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