Brenner, Michael <br/><br/>
A new mutation in GFAP widens the spectrum of Alexander disease.  [electronic resource] 

 -  European journal of human genetics : EJHG  Jan 2015 
 - 1-2 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Comment 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2014.99  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alexander Disease--diagnosis<br/>Codon, Nonsense<br/>Glial Fibrillary Acidic Protein--genetics<br/>Humans<br/>Male<br/>Protein Interaction Domains and Motifs--genetics