Chauveau, Aurélie <br/><br/>
A new point mutation in EPOR inducing a short deletion in congenital erythrocytosis.  [electronic resource] 

 -  British journal of haematology  Feb 2016 
 - 475-7 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>1365-2141 
<br/><br/><label>Standard No.: </label>10.1111/bjh.13511  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Child<br/>Child, Preschool<br/>Female<br/>Gene Deletion<br/>Humans<br/>Janus Kinase 2--genetics<br/>Male<br/>Middle Aged<br/>Point Mutation<br/>Polycythemia--congenital<br/>Receptors, Erythropoietin--genetics<br/>Young Adult