Sarkar, Koustav <br/><br/>
Disruption of hSWI/SNF complexes in T cells by WAS mutations distinguishes X-linked thrombocytopenia from Wiskott-Aldrich syndrome.  [electronic resource] 

 -  Blood  Nov 2014 
 - 3409-19 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1528-0020 
<br/><br/><label>Standard No.: </label>10.1182/blood-2014-07-587642  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cell Nucleus--genetics<br/>Cells, Cultured<br/>Chromosomal Proteins, Non-Histone--genetics<br/>Diagnosis, Differential<br/>Genetic Diseases, X-Linked--diagnosis<br/>Humans<br/>Mutation<br/>Promoter Regions, Genetic<br/>T-Lymphocytes--metabolism<br/>Th1 Cells--metabolism<br/>Thrombocytopenia--diagnosis<br/>Transcription Factors--genetics<br/>Wiskott-Aldrich Syndrome--diagnosis<br/>Wiskott-Aldrich Syndrome Protein--genetics