Shiba, Norio <br/><br/>
DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia.  [electronic resource] 

 -  British journal of haematology  Feb 2012 
 - 413-4 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2141 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2141.2011.08879.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acute Disease<br/>Adolescent<br/>Age of Onset<br/>Bone Marrow Cells--metabolism<br/>Child<br/>Child, Preschool<br/>DNA (Cytosine-5-)-Methyltransferases--genetics<br/>DNA Methyltransferase 3A<br/>Exons--genetics<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Japan--epidemiology<br/>Leukemia, Myeloid--epidemiology<br/>Leukemia, Myelomonocytic, Juvenile--epidemiology<br/>Male<br/>Myelodysplastic Syndromes--epidemiology<br/>Neoplasms, Second Primary--epidemiology<br/>Nuclear Proteins--genetics<br/>Nucleophosmin<br/>RNA, Messenger--genetics<br/>RNA, Neoplasm--genetics<br/>fms-Like Tyrosine Kinase 3--genetics