Lan, Min-Yu <br/><br/>
A novel APP mutation (D678H) in a Taiwanese patient exhibiting dementia and cerebral microvasculopathy.  [electronic resource] 

 -  Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia  Mar 2014 
 - 513-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1532-2653 
<br/><br/><label>Standard No.: </label>10.1016/j.jocn.2013.03.038  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amyloid beta-Protein Precursor--genetics<br/>Asian People--genetics<br/>Base Sequence<br/>Cerebral Amyloid Angiopathy--genetics<br/>Dementia--genetics<br/>Humans<br/>Magnetic Resonance Imaging<br/>Male<br/>Middle Aged<br/>Mutation, Missense