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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Hlavní autoři: Gulez, Nesrin, Aksu, Guzide, Berdeli, Afig, Karaca, Neslihan, Tanrıverdi, Sema, Kutukculer, Necil, Azarsiz, Elif
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi Publishing Corporation 2011
Témata:
Case Report
On-line přístup: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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