Peoc'h, Katell <br/><br/>
Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders.  [electronic resource] 

 -  Human molecular genetics  Dec 2012 
 - 5417-28 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/dds377  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Cloning, Molecular<br/>Creutzfeldt-Jakob Syndrome--genetics<br/>Gerstmann-Straussler-Scheinker Disease--genetics<br/>Humans<br/>Models, Molecular<br/>Molecular Dynamics Simulation<br/>Mutation<br/>Phenotype<br/>Phosphorylation<br/>Plaque, Amyloid--genetics<br/>Prions--genetics<br/>Protein Conformation