Wu, Ye <br/><br/>
Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease.  [electronic resource] 

 -  Journal of human genetics  Feb 2009 
 - 74-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1435-232X 
<br/><br/><label>Standard No.: </label>10.1038/jhg.2008.10  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Asian People--genetics<br/>Child<br/>Child, Preschool<br/>Conserved Sequence<br/>DNA Mutational Analysis<br/>Eukaryotic Initiation Factor-2B--chemistry<br/>Female<br/>Humans<br/>Infant<br/>Leukoencephalopathies--genetics<br/>Magnetic Resonance Imaging<br/>Male<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Mutation, Missense--genetics