Reid, E <br/><br/>
A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13.  [electronic resource] 

 -  American journal of human genetics  Feb 2000 
 - 728-32 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/302783  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Child<br/>Child, Preschool<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 19--genetics<br/>Female<br/>Genes, Dominant--genetics<br/>Genetic Heterogeneity<br/>Haplotypes--genetics<br/>Humans<br/>Lod Score<br/>Male<br/>Microsatellite Repeats--genetics<br/>Paraplegia--epidemiology<br/>Pedigree<br/>Penetrance