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B cell repertoire in patients with a novel BTK mutation: expanding the spectrum of atypical X-linked agammaglobulinemia |
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| Authors: | Toker Ori Broides Arnon Lev Atar Simon Amos J. Megged Orli Shamriz Oded Tal Yuval Somech Raz Lee Yu Nee Nahum Amit |
| Affiliation: | 1.Faculty of Medicine, The Allergy and Immunology Unit, Hebrew University of Jerusalem, Shaare Zedek Medical Center, 12 Bayit Street, 91031, Jerusalem, Israel ;2.Immunology Clinic, Soroka University Medical Center, Beer-Sheva, Israel ;3.Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel ;4.Pediatric Department A and the Immunology Service, Sackler” Faculty of Medicine, Jeffrey Modell Foundation Center; “Edmond and Lily Safra” Children’s Hospital, Sheba Medical Center, Tel Aviv University, Tel-Aviv, Israel ;5.Faculty of Medicine, The Pediatric Infectious Diseases Unit, Hebrew University of Jerusalem, Shaare Zedek Medical Center, Jerusalem, Israel ;6.The Lautenberg Center for Immunology and Cancer Research, Faculty of Medicine, Institute of Medical Research Israel-Canada, Hebrew University of Jerusalem, Jerusalem, Israel ;7.Allergy and Clinical Immunology Unit, Department of Medicine, Faculty of Medicine, Hadassah Medical Organization, Hebrew University of Jerusalem, Jerusalem, Israel ;8.Pediatrics Department A, Soroka University Medical Center, Beer Sheva, Israel ; |
| Abstract: | Immunologic Research - X-linked agammaglobulinemia (XLA) is caused by mutations in the Bruton tyrosine kinase) BTK) gene. Affected patients have severely reduced amounts of circulating B cells.... |
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