Forrest, Shelley L <br/><br/>
Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies.  [electronic resource] 

 -  Brain : a journal of neurology  02 2018 
 - 521-534 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2156 
<br/><br/><label>Standard No.: </label>10.1093/brain/awx328  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Cohort Studies<br/>Correlation of Data<br/>Female<br/>Frontotemporal Dementia--complications<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Tauopathies--complications<br/>tau Proteins--genetics