Chapman, J <br/><br/>
Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.  [electronic resource] 

 -  Neurology  Mar 1996 
 - 758-61 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.46.3.758  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amyloid--genetics<br/>Brain--pathology<br/>Codon<br/>Creutzfeldt-Jakob Syndrome--complications<br/>Fatal Outcome<br/>Female<br/>Humans<br/>Middle Aged<br/>Mutation<br/>Prion Diseases--complications<br/>Prion Proteins<br/>Prions<br/>Protein Precursors--genetics<br/>Sleep Initiation and Maintenance Disorders--genetics