Preethish-Kumar, Veeramani <br/><br/>
CARASIL families from India with 3 novel null mutations in the   [electronic resource] 

 -  Neurology  12 2017 
 - 2392-2394 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/WNL.0000000000004710  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Alopecia--diagnostic imaging<br/>Cerebral Infarction--diagnostic imaging<br/>Female<br/>High-Temperature Requirement A Serine Peptidase 1--genetics<br/>Humans<br/>India<br/>Leukoencephalopathies--diagnostic imaging<br/>Loss of Function Mutation--genetics<br/>Male<br/>Middle Aged<br/>Pedigree<br/>Phenotype<br/>Spinal Diseases--diagnostic imaging<br/>Young Adult