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[Hyper IgM syndrome (HIGM), characterized by recurrent infections, low serum IgG and IgA, normal or elevated IgM, defective class switch recombination and somatic hypermutation, are heterogeneous disorders with at least 6 distinct molecular defects, including the CD40 ligand (CD40L) and the nuclear factor ?B essential modulator (NEMO, also known as IKK?) genes (both X-linked), the CD40, activation-induced cytidine deaminase (AICDA or AID), uracil-DNA glycosylase genes (autosomal recessive) and I?B? (IKBA) (autosomal dominant).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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