Two new missense mutations (P134T and A244V) in the coagulation factor VII gene

This publication has 15 references indexed in Scilit:

• A missense mutation (¹⁷⁸Cys↑Tyr) and two neutral dimorphisms (¹¹⁵His and ³³³Ser) in the human coagulation factor VII gene
  Human Molecular Genetics, 1993
• The β⁺ IVS, I‐NT no. 6 (T→C) thalassaemia in heterozygotes with an associated Hb Valletta or Hb S heterozygosity in homozygotes from Malta
  British Journal of Haematology, 1993
• Nucleotide sequence of the gene for human prothrombin
  Biochemistry, 1987
• Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation.
  Proceedings of the National Academy of Sciences, 1987
• Gene for human factor X: a blood coagulation factor whose gene organization is essentially identical with that of factor IX and protein C
  Biochemistry, 1986
• The nucleotide sequence of the gene for human protein C.
  Proceedings of the National Academy of Sciences, 1985
• Complete nucleotide sequences of the gene for human factor IX (antihemophilic factor B)
  Biochemistry, 1985
• Cloning and sequencing of liver cDNA coding for bovine protein C.
  Proceedings of the National Academy of Sciences, 1984
• DNA sequencing with chain-terminating inhibitors
  Proceedings of the National Academy of Sciences, 1977
• CONGENITAL SPCA DEFICIENCY: A HITHERTO UNRECOGNIZED COAGULATION DEFECT WITH HEMORRHAGE RECTIFIED BY SERUM AND SERUM FRACTIONS 1
  Journal of Clinical Investigation, 1951