Phenotypic approaches to gene mapping in platelet function disorders - identification of new variant of P2Y12, TxA2 and GPVI receptors - Watson, S; Daly, M; Dawood, B; Gissen, P; Makris, M; Mundell, S; Wilde, J; Mumford, A (Hämostaseologie, 2010)
Keywords: Blood Platelet Disorders - genetics; Chromosome Mapping - methods; Gene Expression Regulation; Genetic Association Studies; Hemorrhage - blood; Hemorrhage - genetics; Humans; Phenotype; Platelet Membrane Glycoproteins - genetics; Receptors, Purinergic P2 - genetics; Receptors, Purinergic P2Y12; Receptors, Thromboxane A2, Prostaglandin H2 - genetics