Matsubara-Tsutsui, Miho <br/><br/>
Molecular evidence of presenilin 1 mutation in familial early onset dementia.  [electronic resource] 

 -  American journal of medical genetics  Apr 2002 
 - 292-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.10250  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Alzheimer Disease--genetics<br/>Amino Acid Sequence<br/>Base Sequence<br/>DNA--chemistry<br/>DNA Mutational Analysis<br/>Dementia--genetics<br/>Fatal Outcome<br/>Female<br/>Humans<br/>Male<br/>Membrane Proteins--genetics<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutation<br/>Mutation, Missense<br/>Pedigree<br/>Presenilin-1<br/>Sequence Homology, Amino Acid