The molecular genetics of haemostasis and its inherited disorders /
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| Other Authors: | |
| Format: | Book |
| Language: | English |
| Published: |
Oxford ; New York :
Oxford University Press,
1994.
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| Series: | Oxford medical publications.
Oxford monographs on medical genetics ; no. 25. |
| Subjects: |
Table of Contents:
- Introduction
- Factor VIII and haemophilia A
- Factor IX and haemophilia B
- Factor VII
- Factor X
- Prothrombin
- Protein C and protein C inhibitor
- Protein S, C4b-binding protein, and protein Z
- Thrombomodulin
- Factor V
- Tissue factor
- Tissue factor pathway inhibitor
- Factor XI
- Factor XII
- High-molecular-weight kininogen
- Plasma pre-kallikrein
- Fibrinogen
- Factor XIII
- Antithrombin III
- Heparin cofactor II
- C1 inhibitor
- Histidine-rich glycoprotein
- Placental anticoagulant proteins
- Plasminogen
- Tissue plasminogen activator
- Plasminogen activator inhibitor-1
- Plasminogen activator inhibitor-2
- Urokinase and its receptor
- a₂-antiplasmin
- Von Willebrand factor and Von Willebrand disease
- Platelet membrane proteins
- Platelet-secreted proteins
- Thrombospondin
- Phenotype analysis
- Methodology of mutation detection
- Epidemiology of coagulation disorders.