Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene. [electronic resource]
Producer: 20010412Description: 1131-3 p. digitalISSN:- 0006-4971
- Carrier Proteins -- genetics
- Cohort Studies
- DNA Mutational Analysis
- Diagnosis, Differential
- Epstein-Barr Virus Infections -- complications
- Exons -- genetics
- Genetic Heterogeneity
- Germ-Line Mutation
- Histiocytosis, Non-Langerhans-Cell -- diagnosis
- Humans
- Intracellular Signaling Peptides and Proteins
- Lymphoproliferative Disorders -- diagnosis
- Male
- Sequence Deletion
- Signaling Lymphocytic Activation Molecule Associated Protein
- X Chromosome -- genetics
- src Homology Domains
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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