Novel molecular defect in the platelet ADP receptor P2Y12 of a patient with haemorrhagic diathesis.

Remijn, Jasper A

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

Publication Type: Case Reports; Journal Article

1434-6621

10.1515/CCLM.2007.036 doi


Adult
Blood Platelet Disorders
Collagen
DNA Mutational Analysis
Hemorrhagic Disorders--diagnosis
Humans
Male
Mutation, Missense
Perfusion
Platelet Aggregation
Platelet Function Tests
Receptors, Purinergic P2--deficiency
Receptors, Purinergic P2Y12