Hyper-IgM syndrome type 4 with a B lymphocyte–intrinsic selective deficiency in Ig class-switch recombination

Hyper-IgM syndrome (HIGM) is a heterogeneous condition characterized by impaired Ig class-switch recombination (CSR). The molecular defects that have so far been associated with this syndrome — which affect the CD40 ligand in HIGM type 1 (HIGM1), CD40 in HIGM3, and activation-induced cytidine deamin...

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Autores principales: Imai, Kohsuke, Catalan, Nadia, Plebani, Alessandro, Maródi, László, Sanal, Özden, Kumaki, Satoru, Nagendran, Vasantha, Wood, Philip, Glastre, Catherine, Sarrot-Reynauld, Françoise, Hermine, Olivier, Forveille, Monique, Revy, Patrick, Fischer, Alain, Durandy, Anne
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society for Clinical Investigation 2003
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC162294/
https://ncbi.nlm.nih.gov/pubmed/12840068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200318161
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