Kunishima, S <br/><br/>
De novo mutation of the platelet glycoprotein Ib alpha gene in a patient with pseudo-von Willebrand disease.  [electronic resource] 

 -  Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis  Jul 1997 
 - 311-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0957-5235 
<br/><br/><label>Standard No.: </label>10.1097/00001721-199707000-00009  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Humans<br/>Male<br/>Mutation<br/>Platelet Glycoprotein GPIb-IX Complex--genetics<br/>von Willebrand Diseases--diagnosis