Liu, Zhenwei <br/><br/>
Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing.  [electronic resource] 

 -  Molecular neurobiology  03 2018 
 - 2483-2493 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1559-1182 
<br/><br/><label>Standard No.: </label>10.1007/s12035-017-0483-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>DNA (Cytosine-5-)-Methyltransferases--genetics<br/>DNA Methyltransferase 3A<br/>Databases, Genetic<br/>Gene Regulatory Networks--genetics<br/>Humans<br/>Infant, Newborn<br/>Mutation--genetics<br/>Spasms, Infantile--diagnosis<br/>Exome Sequencing--methods