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Authors
Sullivan, John L.Document Type
Journal ArticlePublication Date
1999-08-01Keywords
Carrier ProteinsCloning, Molecular
*Genetic Linkage
Humans
*Intracellular Signaling Peptides and Proteins
Lymphoproliferative Disorders
Mutation
*X Chromosome
*src Homology Domains
Immunology and Infectious Disease
Pediatrics
Metadata
Show full item recordAbstract
The gene defect responsible for X-linked lymphoproliferative syndrome, SH2D1A (SH2-domain-containing gene 1A), was recently cloned. This gene encodes a small protein of 128 amino acids containing a single SH2 domain, which is thought to play an important role in signal transduction in activated T cells. The definition of SH2D1A protein function will provide insight into the pathogenesis of fatal Epstein-Barr virus infection, lymphomas, Hodgkins disease, immunodeficiency, aplastic anemia and lymphohistiocytic disorders that characterize the syndrome.Source
Curr Opin Immunol. 1999 Aug;11(4):431-4. Link to article on publisher's siteDOI
10.1016/S0952-7915(99)80072-7Permanent Link to this Item
http://hdl.handle.net/20.500.14038/43488PubMed ID
10448142Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1016/S0952-7915(99)80072-7