Clinical flow cytometric screening of SAP and XIAP expression accurately identifies patients withSH2D1AandXIAP/BIRC4mutations
Author:
Affiliation:
1. Division of Bone Marrow Transplantation and Immune Deficiency; Cincinnati Children's Hospital Medical Center; Cincinnati Ohio
2. Division of Human Genetics; Cincinnati Children's Hospital Medical Center; Cincinnati Ohio
Publisher
Wiley
Subject
Cell Biology,Histology,Pathology and Forensic Medicine
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3. Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome;Nichols;Proc Natl Acad Sci USA,1998
4. XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome;Rigaud;Nature,2006
5. How I treat hemophagocytic lymphohistiocytosis;Jordan;Blood,2011
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