Bouslam, Naima <br/><br/>
Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).  [electronic resource] 

 -  Annals of neurology  Apr 2005 
 - 567-71 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0364-5134 
<br/><br/><label>Standard No.: </label>10.1002/ana.20416  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 14<br/>Female<br/>Humans<br/>Lod Score<br/>Male<br/>Microsatellite Repeats<br/>Middle Aged<br/>Morocco<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Spastic Paraplegia, Hereditary--genetics