Roeber, Sigrun <br/><br/>
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.  [electronic resource] 

 -  Acta neuropathologica  Apr 2005 
 - 443-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0001-6322 
<br/><br/><label>Standard No.: </label>10.1007/s00401-004-0978-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Arginine--genetics<br/>Blotting, Western--methods<br/>Brain--metabolism<br/>Creutzfeldt-Jakob Syndrome--genetics<br/>DNA Mutational Analysis--methods<br/>Female<br/>Histidine--genetics<br/>Histological Techniques--methods<br/>Humans<br/>Immunohistochemistry--methods<br/>Molecular Weight<br/>Mutation<br/>Prions--genetics