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    • Defective lymphoid organogenesis underlies the immune deficiency caused by a heterozygous S32I mutation in IκBα 

      Mooster, Jana L.; Le Bras, Severine; Massaad, Michel J.; Jabara, Haifa; Yoon, Juhan; Galand, Claire; Heesters, Balthasar A.; Burton, Oliver T.; Mattoo, Hamid; Manis, John; Geha, Raif S. (The Rockefeller University Press, 2015)
      Patients with ectodermal dysplasia with immunodeficiency (ED-ID) caused by mutations in the inhibitor of NF-κB α (IκBα) are susceptible to severe recurrent infections, despite normal T and B cell numbers and intact in vitro ...