XLP: Clinical Features and Molecular Etiology due to Mutations in SH2D1A Encoding SAP

Journal of Clinical Immunology

Volumn 34, Issue 7, 2014, Pages 772-779

  Tangye, Stuart G ^a,b  

^a GARVAN INSTITUTE OF MEDICAL RESEARCH   (Australia)

^b UNIVERSITY OF NEW SOUTH WALES   (Australia)

Author keywords

EBV; hypogammaglobulinemia; infectious mononucleosis; lymphoma; PID; SAP; XLP

Indexed keywords

SH2D1A PROTEIN, HUMAN; SIGNAL PEPTIDE;

COMPLICATION; EPSTEIN BARR VIRUS; EPSTEIN-BARR VIRUS INFECTIONS; GENETICS; HUMAN; HUMORAL IMMUNITY; IMMUNOLOGY; LYMPHOMA, B-CELL; LYMPHOPOIESIS; LYMPHOPROLIFERATIVE DISEASE; METABOLISM; MUTATION; NATURAL KILLER CELL; PHYSIOLOGY; SIGNAL TRANSDUCTION; T LYMPHOCYTE;

EPSTEIN-BARR VIRUS INFECTIONS; HERPESVIRUS 4, HUMAN; HUMANS; IMMUNITY, HUMORAL; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; KILLER CELLS, NATURAL; LYMPHOMA, B-CELL; LYMPHOPOIESIS; LYMPHOPROLIFERATIVE DISORDERS; MUTATION; SIGNAL TRANSDUCTION; T-LYMPHOCYTES;

EID: 84930898417     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-014-0083-7     Document Type: Review

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