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

類似資料

• An intragenic deletion of the factor IX gene in a family with hemophilia B.
  著者:: Chen, S H, 等
  出版事項: (1985)
• Partial factor IX protein in a pedigree with hemophilia B due to a partial gene deletion.
  著者:: Bray, G L, 等
  出版事項: (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.
  著者:: Higuchi, M, 等
  出版事項: (1991)
• Factor IX antigen by radioimmunoassay. Abnormal factor IX protein in patients on warfarin therapy and with hemophilia B.
  著者:: Thompson, A R
  出版事項: (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.
  著者:: Chen, S H, 等
  出版事項: (1989)