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T<sup>+</sup> NK<sup>+</sup> IL-2 Receptor γ Chain Mutation: a Challenging Diagnosis of Atypical Severe Combined Immunodeficiency.

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第一作者: Polina,Stepensky
第一单位: Department of Bone Marrow Transplantation and Cancer Immunotherapy, Hadassah-Hebrew University Hospital, POB 12000, 91200, Jerusalem, Israel. polina@hadassah.org.il.
作者单位: Department of Bone Marrow Transplantation and Cancer Immunotherapy, Hadassah-Hebrew University Hospital, POB 12000, 91200, Jerusalem, Israel. polina@hadassah.org.il. [1] Center for Chronic Immunodeficiency (CCI), University Medical Center Freiburg and Faculty of Medicine, University of Freiburg, Freiburg, Germany. [2] Pediatric Division, Hadassah-Hebrew University Medical Center, Jerusalem, Israel. [3] Department of Bone Marrow Transplantation and Cancer Immunotherapy, Hadassah-Hebrew University Hospital, POB 12000, 91200, Jerusalem, Israel.;Immunology Division, Garvan Institute of Medical Research, Sydney, Australia.;Graduate Research School, The University of New South Wales, Sydney, Australia. [4] Department of Bone Marrow Transplantation and Cancer Immunotherapy, Hadassah-Hebrew University Hospital, POB 12000, 91200, Jerusalem, Israel. [5] Pediatric Department, Makassed Hospital, Jerusalem, Israel. [6] Department of Dermatology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel. [7] Nablus Specialty Hospital, Palestinian Authority, Nablus, Palestine. [8] Pediatric Department A and the Immunology Services, "Edmond and Lily Safra" Children's Hospital, Jeffrey Modell Foundation Center, Sheba Medical Center, Tel Hashomer affiliated with Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel. [9] Monique and Jacques Roboh Department of Genetic Research, Hadassah, Hebrew University Medical Center, Jerusalem, Israel. [10]
DOI 10.1007/s10875-018-0514-y
PMID 29948574
发布时间 2019-10-14
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Journal of clinical immunology

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