Kaykçoğlu, Meral <br/><br/>
Homozygous factor V Leiden mutation in two siblings presenting with acute myocardial infarction: a rare cause of myocardial infarction in the young.  [electronic resource] 

 -  Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis  Jun 2005 
 - 281-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0957-5235 
<br/><br/><label>Standard No.: </label>10.1097/01.mbc.0000169221.38797.9c  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Coronary Angiography<br/>Coronary Thrombosis--diagnostic imaging<br/>Electrocardiography<br/>Factor V--genetics<br/>Genetic Predisposition to Disease<br/>Homozygote<br/>Humans<br/>Male<br/>Myocardial Infarction--genetics<br/>Pedigree<br/>Point Mutation<br/>Siblings