Haemophilia B: database of point mutations and short additions and deletions--second edition

This publication has 55 references indexed in Scilit:

• THE PATTERN OF FACTOR-IX GERM-LINE MUTATION IN ASIANS IS SIMILAR TO THAT OF CAUCASIANS
  1990
• THE PUTATIVE FACTOR-IX GENE PROMOTER IN HEMOPHILIA-B LEYDEN
  1988
• GENETIC-DEFECT RESPONSIBLE FOR THE DYSFUNCTIONAL PROTEIN - FACTOR-IXLONG BEACH
  1988
• Haemophilia B+ with Inhibitor
  Thrombosis and Haemostasis, 1988
• Hemophilia B (factor IXSeattle 2) due to a single nucleotide deletion in the gene for factor IX.
  Journal of Clinical Investigation, 1987
• Hemophilia B (Christmas disease) variants and carrier detection analyzed by DNA probes.
  Journal of Clinical Investigation, 1987
• FACTOR-IXALABAMA - A POINT MUTATION IN A CLOTTING PROTEIN RESULTS IN HEMOPHILIA-B
  1987
• Molecular basis of hemophilia B: a defective enzyme due to an unprocessed propeptide is caused by a point mutation in the factor IX precursor.
  Proceedings of the National Academy of Sciences, 1986
• Defective propeptide processing of blood clotting factor IX caused by mutation of arginine to glutamine at position −4
  Cell, 1986
• Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145.
  Proceedings of the National Academy of Sciences, 1983