Haemophilia B caused by mutation of a potential thrombin cleavage site in factor IX.

Antzeko izenburuak

• A factor IX mutation, verified by direct genomic sequencing, causes haemophilia B by a novel mechanism.
  nork: Tsang, T C, et al.
  Argitaratua: (1988)
• A less severe form of Haemophilia B Leyden.
  nork: Crossley, M, et al.
  Argitaratua: (1990)
• Factor IX(Basel): a Swiss family with severe haemophilia B having a point mutation in EGF type B domain
  Argitaratua: (1991)
• Interaction of thrombin with PAR1 and PAR4 at the thrombin cleavage site
  nork: Nieman, Marvin T., et al.
  Argitaratua: (2007)
• Direct characterization of factor VIII in plasma: detection of a mutation altering a thrombin cleavage site (arginine-372----histidine).
  nork: Arai, M, et al.
  Argitaratua: (1989)