Splice junction mutations in factor IX gene resulting in severe hemophilia B

Ítems similars

• An intragenic deletion of the factor IX gene in a family with hemophilia B.
  per: Chen, S H, et al.
  Publicat: (1985)
• Partial factor IX protein in a pedigree with hemophilia B due to a partial gene deletion.
  per: Bray, G L, et al.
  Publicat: (1986)
• Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene.
  per: Higuchi, M, et al.
  Publicat: (1991)
• Factor IX antigen by radioimmunoassay. Abnormal factor IX protein in patients on warfarin therapy and with hemophilia B.
  per: Thompson, A R
  Publicat: (1977)
• Three point mutations in the factor IX genes of five hemophilia B patients. Identification strategy using localization by altered epitopes in their hemophilic proteins.
  per: Chen, S H, et al.
  Publicat: (1989)