Basset-Leobon, Céline <br/><br/>
Familial Creutzfeldt-Jakob disease with an R208H-129V haplotype and Kuru plaques.  [electronic resource] 

 -  Archives of neurology  Mar 2006 
 - 449-52 p.  digital 
<br/><br/> Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0003-9942 
<br/><br/><label>Standard No.: </label>10.1001/archneur.63.3.449  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amyloid--genetics<br/>Arginine--genetics<br/>Blotting, Western--methods<br/>Brain--pathology<br/>Creutzfeldt-Jakob Syndrome--genetics<br/>Haplotypes<br/>Histidine--genetics<br/>Humans<br/>Immunohistochemistry--methods<br/>Male<br/>Middle Aged<br/>Mutation<br/>Plaque, Amyloid--pathology<br/>Prion Proteins<br/>Prions<br/>Protein Precursors--genetics<br/>Valine--genetics