Zhao, Meina <br/><br/>
A novel XIAP mutation in a Japanese boy with recurrent pancytopenia and splenomegaly.  [electronic resource] 

 -  Haematologica  Apr 2010 
 - 688-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1592-8721 
<br/><br/><label>Standard No.: </label>10.3324/haematol.2009.018010  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Female<br/>Flow Cytometry<br/>Humans<br/>Lymphocytes--metabolism<br/>Male<br/>Mothers<br/>Mutation--genetics<br/>Pancytopenia--genetics<br/>Recurrence<br/>Splenomegaly--genetics<br/>X-Linked Inhibitor of Apoptosis Protein--genetics