Doran, Mark <br/><br/>
Familial early-onset dementia with tau intron 10 + 16 mutation with clinical features similar to those of Alzheimer disease.  [electronic resource] 

 -  Archives of neurology  Oct 2007 
 - 1535-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0003-9942 
<br/><br/><label>Standard No.: </label>10.1001/archneur.64.10.1535  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Alzheimer Disease--psychology<br/>Atrophy<br/>Cerebral Cortex--pathology<br/>Dementia--genetics<br/>Disease Progression<br/>Family<br/>Fatal Outcome<br/>Female<br/>Hippocampus--pathology<br/>Humans<br/>Introns--genetics<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Neuropsychological Tests<br/>Pedigree<br/>tau Proteins--genetics