Chang, Ki-Eun <br/><br/>
Type II (adult onset) Alexander disease in a paraplegic male with a rare D128N mutation in the GFAP gene.  [electronic resource] 

 -  Clinical neuropathology   
 - 298-302 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0722-5091 
<br/><br/><label>Standard No.: </label>10.5414/NP300863  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alexander Disease--complications<br/>Glial Fibrillary Acidic Protein--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Paraplegia--complications