He, Ruojie <br/><br/>
Homozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report.  [electronic resource] 

 -  BMC neurology  Mar 2020 
 - 72 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1471-2377 
<br/><br/><label>Standard No.: </label>10.1186/s12883-020-01660-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Asian People--genetics<br/>Brain--pathology<br/>CADASIL--genetics<br/>Homozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Pedigree<br/>Receptor, Notch3--genetics