Lossos, Alexander <br/><br/>
Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity.  [electronic resource] 

 -  Archives of neurology  May 2006 
 - 756-60 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0003-9942 
<br/><br/><label>Standard No.: </label>10.1001/archneur.63.5.756  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Agenesis of Corpus Callosum<br/>Chromosomes, Human, Pair 15--genetics<br/>Corpus Callosum--pathology<br/>DNA Mutational Analysis--methods<br/>Family Health<br/>Female<br/>Genetic Heterogeneity<br/>Genetic Linkage<br/>Humans<br/>Magnetic Resonance Imaging--methods<br/>Male<br/>Membrane Proteins--classification<br/>Pedigree<br/>Spastic Paraplegia, Hereditary--genetics