Reid, E <br/><br/>
Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.  [electronic resource] 

 -  Neurology  Nov 1999 
 - 1844-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.53.8.1844  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 8<br/>Female<br/>Genes, Dominant<br/>Genetic Variation<br/>Humans<br/>Lod Score<br/>Male<br/>Middle Aged<br/>Paraplegia--genetics<br/>Pedigree<br/>Phenotype