Uyama, E <br/><br/>
Arg133Cys mutation of Notch3 in two unrelated Japanese families with CADASIL.  [electronic resource] 

 -  Internal medicine (Tokyo, Japan)  Sep 2000 
 - 732-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0918-2918 
<br/><br/><label>Standard No.: </label>10.2169/internalmedicine.39.732  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Arginine--genetics<br/>Brain--pathology<br/>Cystine--genetics<br/>DNA Mutational Analysis<br/>DNA Primers--chemistry<br/>Dementia, Multi-Infarct--diagnosis<br/>Female<br/>Humans<br/>Japan--epidemiology<br/>Magnetic Resonance Imaging<br/>Male<br/>Middle Aged<br/>Pedigree<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Polymorphism, Single-Stranded Conformational<br/>Proto-Oncogene Proteins--genetics<br/>Receptor, Notch3<br/>Receptors, Cell Surface<br/>Receptors, Notch<br/>Sequence Analysis, DNA