Xia, Jun <br/><br/>
Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia.  [electronic resource] 

 -  British journal of haematology  Nov 2009 
 - 535-42 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2141 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2141.2009.07888.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing<br/>Chronic Disease<br/>DNA Mutational Analysis--methods<br/>DNA-Binding Proteins--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Genotype<br/>Glucose-6-Phosphatase--genetics<br/>Humans<br/>Leukocyte Elastase--genetics<br/>Male<br/>Mutation<br/>Neutropenia--congenital<br/>Proteins--genetics<br/>Transcription Factors--genetics<br/>Wiskott-Aldrich Syndrome Protein--genetics