Rossi, Giacomina <br/><br/>
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  Apr 2008 
 - 892-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1531-8257 
<br/><br/><label>Standard No.: </label>10.1002/mds.21970  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Amino Acid Substitution<br/>Basal Ganglia--pathology<br/>Brain Diseases--genetics<br/>Cerebral Cortex--pathology<br/>Chromosomes, Human, Pair 17<br/>Dementia--genetics<br/>Humans<br/>Male<br/>Parkinson Disease--genetics<br/>Tauopathies--genetics<br/>Tremor--etiology<br/>tau Proteins--genetics