Partial factor IX protein in a pedigree with hemophilia B due to a partial gene deletion.

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)
• Hemophilia B (factor IXSeattle 2) due to a single nucleotide deletion in the gene for factor IX.
  著者:: Schach, B G, 等
  出版事項: (1987)
• Splice junction mutations in factor IX gene resulting in severe hemophilia B
  著者:: Chen, S.-H., 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)
• Identification and Genetic Analysis of a Factor IX Gene Intron 3 Mutation in a Hemophilia B Pedigree in China
  著者:: Cao, Dong-Hua, 等
  出版事項: (2014)