Warner, D <br/><br/>
The thrombomodulin gene mutation G(127)-->A (Ala25Thr) and cerebrovascular disease.  [electronic resource] 

 -  Cerebrovascular diseases (Basel, Switzerland)   
 - 359-63 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1015-9770 
<br/><br/><label>Standard No.: </label>10.1159/000016091  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Aged, 80 and over<br/>Cerebrovascular Disorders--epidemiology<br/>Female<br/>Genetic Predisposition to Disease<br/>Humans<br/>Male<br/>Middle Aged<br/>Point Mutation<br/>Risk Factors<br/>Thrombomodulin--genetics