Poulain, Stéphanie <br/><br/>
MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome.  [electronic resource] 

 -  British journal of haematology  Nov 2014 
 - 506-13 p.  digital 
<br/><br/> Publication Type: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2141 
<br/><br/><label>Standard No.: </label>10.1111/bjh.13078  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Bone Marrow--metabolism<br/>Heterozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>Myeloid Differentiation Factor 88--genetics<br/>Neoplasm Proteins--genetics<br/>Nervous System Diseases--cerebrospinal fluid<br/>Prospective Studies<br/>Syndrome<br/>Waldenstrom Macroglobulinemia--cerebrospinal fluid