Remijn, Jasper A <br/><br/>
Novel molecular defect in the platelet ADP receptor P2Y12 of a patient with haemorrhagic diathesis.  [electronic resource] 

 -  Clinical chemistry and laboratory medicine  2007 
 - 187-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1434-6621 
<br/><br/><label>Standard No.: </label>10.1515/CCLM.2007.036  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Blood Platelet Disorders<br/>Collagen<br/>DNA Mutational Analysis<br/>Hemorrhagic Disorders--diagnosis<br/>Humans<br/>Male<br/>Mutation, Missense<br/>Perfusion<br/>Platelet Aggregation<br/>Platelet Function Tests<br/>Receptors, Purinergic P2--deficiency<br/>Receptors, Purinergic P2Y12