Klebe, Stephan <br/><br/>
NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe.  [electronic resource] 

 -  Neurogenetics  Apr 2007 
 - 155-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1364-6745 
<br/><br/><label>Standard No.: </label>10.1007/s10048-006-0074-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Amino Acid Substitution<br/>Child<br/>Europe<br/>Exons<br/>Female<br/>Genes, Dominant<br/>Humans<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation<br/>Paraplegia--genetics