Hanein, Sylvain <br/><br/>
A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.  [electronic resource] 

 -  Human genetics  Nov 2007 
 - 261-73 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s00439-007-0396-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Aged<br/>Child<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 10--genetics<br/>Chromosomes, Human, Pair 8--genetics<br/>Female<br/>Genes, Dominant<br/>Genetic Markers<br/>Haplotypes<br/>Humans<br/>Kinesins--genetics<br/>Lod Score<br/>Male<br/>Microsatellite Repeats<br/>Middle Aged<br/>Nerve Tissue Proteins--genetics<br/>Neuregulin-1<br/>Pedigree<br/>Spastic Paraplegia, Hereditary--genetics