Haplotypes of the endothelial protein C receptor gene and Behçet's disease.
Autores de IIS La Fe
Participantes ajenos a IIS La Fe
- Fontcuberta J
Grupos
Abstract
Behçet's disease is a vasculitis of unknown cause in which thrombosis occurs in about 25% of patients. Two haplotypes of the endothelial protein C receptor gene, H1 and H3, are associated with the risk of thrombosis. Thus, the objective of this study was to evaluate the influence of these haplotypes on the thrombosis risk in Behçet's disease.
Datos de la publicación
- ISSN/ISSNe:
- 0049-3848, 1879-2472
- Tipo:
- Article
- Páginas:
- 459-464
- PubMed:
- 21851971
- Factor de Impacto:
- 1,133 SCImago ℠
- Cuartil:
- Q2 SCImago ℠
THROMBOSIS RESEARCH PERGAMON-ELSEVIER SCIENCE LTD
Citas Recibidas en Web of Science: 7
Documentos
- No hay documentos
Filiaciones
Cita
NAVARRO S,BONET E,MEDINA P,MARTOS L,RICART JM,VAYÁ A,TODOLÍ J,Fontcuberta J,ESTELLÉS A,ESPAÑA F. Haplotypes of the endothelial protein C receptor gene and Behçet's disease. Thromb. Res. 2012. 129. (4):p. 459-464. IF:3,133. (2).
Portal de investigación