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New mutations in exon 28 of the von Willebrand factor gene detected in patients with different types of von Willebrand's disease.
Fecha de publicación:
Autores de IIS La Fe
Participantes ajenos a IIS La Fe
- Tavares A
Abstract
von Willebrand's disease (vWD), the most common hereditary bleeding disorder in humans, is caused by qualitative and/or quantitative deficiencies of von Willebrand factor, and can manifest itself under several different phenotypes. Most of the molecular defects have been detected in qualitative variants involving exon 28 of the vWF gene. Patients from four unrelated families with different types of vWD were included in the mutation screening of this region.
Datos de la publicación
- ISSN/ISSNe:
- 0390-6078, 1592-8721
- Tipo:
- Article
- Páginas:
- 414-419
- PubMed:
- 11325649
- Factor de Impacto:
- 0,507 SCImago ℠
- Cuartil:
- Q2 SCImago ℠
Haematologica-The Hematology Journal FERRATA STORTI FOUNDATION
Citas Recibidas en Web of Science: 20
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Cita
CASAÑA P,MARTÍNEZ F,HAYA S,Tavares A,AZNAR JA. New mutations in exon 28 of the von Willebrand factor gene detected in patients with different types of von Willebrand's disease. Haematol-Hematol. J. 2001. 86. (4):p. 414-419. IF:3,216. (1).