Abstract
RATIONALE: Hyper IgM syndrome (HIGM) is characterized by multiple etiologies including deficiencies in CD40L and CD40 and defects in AID, uracil-N-glycosylase (UNG), NF-κβ essential modulator (NEMO). There are other unknown genetic mutations which result in this phenotype as well.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have