Ashley-Koch, A <br/><br/>
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.  [electronic resource] 

 -  Neurogenetics  Mar 2001 
 - 91-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1364-6745 
<br/><br/><label>Standard No.: </label>10.1007/s100480000098  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 12<br/>Chromosomes, Human, Pair 19<br/>Chromosomes, Human, Pair 2<br/>Chromosomes, Human, Pair 8<br/>Female<br/>Genes, Dominant<br/>Genetic Linkage<br/>Genetic Markers<br/>Genotype<br/>Haplotypes<br/>Humans<br/>Lod Score<br/>Male<br/>Pedigree<br/>Spastic Paraplegia, Hereditary--genetics