Yoon, W T <br/><br/>
Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation.  [electronic resource] 

 -  European journal of neurology  Jan 2012 
 - e7-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1468-1331 
<br/><br/><label>Standard No.: </label>10.1111/j.1468-1331.2011.03569.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Corpus Callosum--pathology<br/>DNA Mutational Analysis<br/>Humans<br/>Korea<br/>Male<br/>Mutation<br/>Proteins--genetics<br/>Spastic Paraplegia, Hereditary--genetics<br/>Young Adult