Sun, Lin <br/><br/>
Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene.  [electronic resource] 

 -  Prion  2015 
 - 228-35 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1933-690X 
<br/><br/><label>Standard No.: </label>10.1080/19336896.2015.1054601  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Brain--pathology<br/>Codon--genetics<br/>Electroencephalography<br/>Female<br/>Homozygote<br/>Humans<br/>Insomnia, Fatal Familial--genetics<br/>Magnetic Resonance Imaging<br/>Male<br/>Methionine--genetics<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Pedigree<br/>Prions--genetics