Identification of mutations in 15 Hungarian families with hereditary protein C deficiency

This publication has 27 references indexed in Scilit:

• Molecular Basis For Protein C Hereditary Deficiency
  Pathophysiology of Haemostasis and Thrombosis, 1996
• Structure-function assessment of the role of the helical stack domain in the properties of human recombinant protein C and activated protein C
  Biochemistry, 1995
• The protein C anticoagulant system: Inherited defects as basis for venous thrombosis
  Thrombosis Research, 1995
• Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis
  The Lancet, 1994
• Mutation in blood coagulation factor V associated with resistance to activated protein C
  Nature, 1994
• Scanning method to establish the molecular basis of protein C deficiencies
  Human Mutation, 1994
• Incidence and clinical characteristics of hereditary disorders associated with venous thrombosis
  American Journal of Hematology, 1991
• Neonatal Purpura Fulminans Due to Homozygous Protein C or Protein S Deficiencies
  Seminars in Thrombosis and Hemostasis, 1990
• Mutations in the catalytic domain of human coagulation factor IX: Rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior
  Genomics, 1989
• Electroimmuno Assay
  Scandinavian Journal of Clinical and Laboratory Investigation, 1972