Arico, M <br/><br/>
Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene.  [electronic resource] 

 -  Blood  Feb 2001 
 - 1131-3 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Standard No.: </label>10.1182/blood.v97.4.1131  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carrier Proteins--genetics<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Diagnosis, Differential<br/>Epstein-Barr Virus Infections--complications<br/>Exons--genetics<br/>Genetic Heterogeneity<br/>Germ-Line Mutation<br/>Histiocytosis, Non-Langerhans-Cell--diagnosis<br/>Humans<br/>Intracellular Signaling Peptides and Proteins<br/>Lymphoproliferative Disorders--diagnosis<br/>Male<br/>Sequence Deletion<br/>Signaling Lymphocytic Activation Molecule Associated Protein<br/>X Chromosome--genetics<br/>src Homology Domains