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Deficiency of innate and acquired immunity caused by an IKBKB mutation.
Pannicke, Ulrich; Baumann, Bernd; Fuchs, Sebastian; Henneke, Philipp; Rensing-Ehl, Anne; Rizzi, Marta; Janda, Ales; Hese, Katrin; Schlesier, Michael; Holzmann, Karlheinz; Borte, Stephan; Laux, Constanze; Rump, Eva-Maria; Rosenberg, Alan; Zelinski, Teresa; Schrezenmeier, Hubert; Wirth, Thomas; Ehl, Stephan; Schroeder, Marlis L; Schwarz, Klaus.
Affiliation
  • Pannicke U; From the Institute for Transfusion Medicine, University Hospital Ulm (U.P., C.L., H.S., K.S.), the Institute of Physiological Chemistry (B.B., T.W.), the Center for Biomedical Research, Genomics Core Facility (K. Holzmann), University of Ulm, and the Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Service Baden-Wuerttemberg-Hessen (E.-M.R., H.S., K.S.), Ulm; the Center of Chronic Immunodeficiency, University Medical Center Freiburg (S.F., P.H., A.R.-E.,
N Engl J Med ; 369(26): 2504-14, 2013 Dec 26.
Article in En | MEDLINE | ID: mdl-24369075

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Severe Combined Immunodeficiency / Agammaglobulinemia / I-kappa B Kinase / Mutation Type of study: Prognostic_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: N Engl J Med Year: 2013 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Severe Combined Immunodeficiency / Agammaglobulinemia / I-kappa B Kinase / Mutation Type of study: Prognostic_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: N Engl J Med Year: 2013 Type: Article