Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
about
Inherited platelet disorders: toward DNA-based diagnosisGenotyping and phenotyping of platelet function disordersCongenital platelet disorders and understanding of platelet function.Impact of vascular thromboxane prostanoid receptor activation on hemostasis, thrombosis, oxidative stress, and inflammation.Rare platelet GPCR variants: what can we learn?Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand Disease.How should we test for nonsevere heritable platelet function disorders?Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors.TBXA2R gene variants associated with bleeding
P2860
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P2860
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
description
2013 nî lūn-bûn
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name
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
@en
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
@nl
type
label
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
@en
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
@nl
prefLabel
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
@en
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
@nl
P2093
P2860
P50
P356
P1476
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant
@en
P2093
A D Mumford
A-M Fischer
F Zinzindohoue
S J Mundell
UK GAPP Study Group
P2860
P304
P356
10.1111/JTH.12117
P577
2013-03-01T00:00:00Z