Haplotypes of the endothelial protein C receptor gene and Behçet's disease.

Fecha de publicación:

Autores de IIS La Fe

  • Silvia Navarro Rosales

    Autor

  • Elena Bonet Estruch

    Autor

  • Laura Martos Marin

    Autor

  • Jose Maria Ricart Vaya

    Autor

  • Amparo Vaya Montañana

    Autor

  • Amparo Estelles Cortes

    Autor

  • Francisco España Furio

    Autor

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

THROMBOSIS RESEARCH  PERGAMON-ELSEVIER SCIENCE LTD

Tipo:
Article
Páginas:
459-464
PubMed:
21851971
Factor de Impacto:
1,133 SCImago
Cuartil:
Q2 SCImago

Citas Recibidas en Web of Science: 7

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