Santa, Yo <br/><br/>
Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis.  [electronic resource] 

 -  Journal of the neurological sciences  Aug 2003 
 - 79-84 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-510X 
<br/><br/><label>Standard No.: </label>10.1016/s0022-510x(03)00109-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age of Onset<br/>Arginine--genetics<br/>Arteries--pathology<br/>Brain--metabolism<br/>Cerebral Arterial Diseases--complications<br/>Cerebral Infarction--complications<br/>Cysteine--genetics<br/>DNA Mutational Analysis<br/>Family Health<br/>Female<br/>Humans<br/>Immunohistochemistry<br/>Japan--epidemiology<br/>Lysine--genetics<br/>Magnetic Resonance Imaging<br/>Male<br/>Microscopy, Electron--methods<br/>Muscular Diseases--complications<br/>Mutation<br/>Phenylalanine--genetics<br/>Proto-Oncogene Proteins--genetics<br/>Receptor, Notch3<br/>Receptors, Cell Surface<br/>Receptors, Notch