Kamimura, K <br/><br/>
Identification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.  [electronic resource] 

 -  Alzheimer disease and associated disorders   
 - 222-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0893-0341 
<br/><br/><label>Standard No.: </label>10.1097/00002093-199910000-00008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Dementia, Multi-Infarct--genetics<br/>Female<br/>Humans<br/>Japan<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation, Missense--genetics<br/>Pedigree<br/>Polymorphism, Single-Stranded Conformational<br/>Receptors, Notch