Lesson from hypomorphic recombination-activating gene (RAG) mutations: Why asymptomatic siblings should also be tested - 29/03/14
Doi : 10.1016/j.jaci.2013.10.021
Catharina Schuetz, MD a, ∗ 
, Ulrich Pannicke, PhD b, ∗, Eva-Maria Jacobsen, PhD a, Siegfried Burggraf, PhD c, Michael H. Albert, MD d, Manfred Hönig, MD a, Tim Niehues, MD e, Oliver Feyen, PhD f, g, Stephan Ehl, MD h, Klaus-Michael Debatin, MD a, Wilhelm Friedrich, MD a, Ansgar S. Schulz, MD a, Klaus Schwarz, MD b, i
, Ulrich Pannicke, PhD b, ∗, Eva-Maria Jacobsen, PhD a, Siegfried Burggraf, PhD c, Michael H. Albert, MD d, Manfred Hönig, MD a, Tim Niehues, MD e, Oliver Feyen, PhD f, g, Stephan Ehl, MD h, Klaus-Michael Debatin, MD a, Wilhelm Friedrich, MD a, Ansgar S. Schulz, MD a, Klaus Schwarz, MD b, i a Department of Pediatrics and Adolescent Medicine, University Hospital Ulm, Ulm, Germany
b Institute for Transfusion Medicine, University of Ulm, Ulm, Germany
c Labor Becker, Olgemöller und Kollegen, Munich, Germany
d Dr von Hauner University Children’s Hospital, Munich, Germany
e Center for Child and Adolescent Health, HELIOS Klinikum Krefeld, Academic Hospital, Heinrich Heine University Düsseldorf, Düsseldorf, Germany
f Department of Pediatric Oncology, Hematology, and Clinical Immunology, Children’s Hospital, University Düsseldorf, Heinrich Heine University, Düsseldorf, Germany
g Tavarlin AG, Darmstadt, Germany
h Centre of Chronic Immunodeficiency, University Hospital Freiburg, Freiburg, Germany
i Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Service, Baden-Württemberg-Hessen, Germany
| Disclosure of potential conflict of interest: The authors declare that they have no relevant conflicts of interest. |
© 2013
American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 133 - N° 4
P. 1211 - avril 2014 Retour au numéro
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