Bernardi, Livia <br/><br/>
Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome.  [electronic resource] 

 -  Neurobiology of aging  Nov 2014 
 - 2657.e7-2657.e11 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1558-1497 
<br/><br/><label>Standard No.: </label>10.1016/j.neurobiolaging.2014.06.006  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Female<br/>Frontotemporal Lobar Degeneration--diagnosis<br/>Genetic Association Studies<br/>Genetic Testing<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>Prions--genetics<br/>Protein Structure, Tertiary--genetics<br/>Syndrome