X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis

The X-linked lymphoproliferative syndrome (XLP) is a rare, inherited immunodeficiency characterized by recurrent episodes of hemophagocytic lymphohistiocytosis, hypogammaglobulinemia, and/or lymphomas. Recently, X-linked inhibitor of apoptosis (XIAP/BIRC4) gene defects, in families with XLP but with...

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書誌詳細
主要な著者: Gulez, Nesrin, Aksu, Guzide, Berdeli, Afig, Karaca, Neslihan, Tanrıverdi, Sema, Kutukculer, Necil, Azarsiz, Elif
フォーマット: Artigo
言語:Inglês
出版事項: Hindawi Publishing Corporation 2011
主題:
Case Report
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3085308/
https://ncbi.nlm.nih.gov/pubmed/21541208
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2011/121258
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