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

Benzer Materyaller

• An intragenic deletion of the factor IX gene in a family with hemophilia B.
  Yazar:: Chen, S H, ve diğerleri
  Baskı/Yayın Bilgisi: (1985)
• 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.
  Yazar:: Higuchi, M, ve diğerleri
  Baskı/Yayın Bilgisi: (1991)
• Partial factor IX protein in a pedigree with hemophilia B due to a partial gene deletion.
  Yazar:: Bray, G L, ve diğerleri
  Baskı/Yayın Bilgisi: (1986)
• Three point mutations in the factor IX genes of five hemophilia B patients. Identification strategy using localization by altered epitopes in their hemophilic proteins.
  Yazar:: Chen, S H, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)
• Factor IX antigen by radioimmunoassay. Abnormal factor IX protein in patients on warfarin therapy and with hemophilia B.
  Yazar:: Thompson, A R
  Baskı/Yayın Bilgisi: (1977)