Oki, K <br/><br/>
Novel mutation of the Notch3 gene in a Japanese patient with CADASIL.  [electronic resource] 

 -  European journal of neurology  Apr 2007 
 - 464-6 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1468-1331 
<br/><br/><label>Standard No.: </label>10.1111/j.1468-1331.2007.01641.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Asian People<br/>Brain--pathology<br/>CADASIL--diagnosis<br/>Diagnosis, Differential<br/>Female<br/>Humans<br/>Magnetic Resonance Angiography<br/>Magnetic Resonance Imaging<br/>Male<br/>Meniere Disease--diagnosis<br/>Microscopy, Electron, Transmission<br/>Mutation, Missense<br/>Pedigree<br/>Receptor, Notch3<br/>Receptors, Notch--genetics<br/>Skin--pathology<br/>Tinnitus--physiopathology<br/>Vertigo--physiopathology