Hereditary deficiency of vitamin K-dependent coagulation factors

Thrombosis and Haemostasis

Volumn 84, Issue 6, 2000, Pages 935-936

  Brenner, B ^a  

^a RAMBAM MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIVITAMIN K; BLOOD CLOTTING FACTOR; BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 9; OSTEOCALCIN; PROTEIN C; PROTEIN S; PROTHROMBIN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE (PHOSPHATE) DEHYDROGENASE (QUINONE); VITAMIN K DEPENDENT CARBOXYLASE; VITAMIN K GROUP; WARFARIN;

BINDING KINETICS; BLEEDING DISORDER; CLINICAL FEATURE; DISEASE ASSOCIATION; DNA SEQUENCE; DNA SYNTHESIS; DRUG DEGRADATION; FUNCTIONAL ASSESSMENT; GENE MUTATION; HUMAN; MOLECULAR INTERACTION; NOTE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; THROMBOCYTE VOLUME; VITAMIN K DEFICIENCY;

EID: 0034530568     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1614151     Document Type: Note

References (17)

1. Characterization of the γ-glutamyl carboxylase
2. Congenital combined deficiency of coagulation factors II, VII, IX and X
3. Studies on a family with combined functional deficiencies of vitamin K-dependent coagulation factors
4. Congenital deficiency of vitamin K-dependent coagulation factors and protein C
5. Hereditary deficiency of all vitamin K-dependent procoagulants and anticoagulants
6. Association of congenital deficiency of multiple vitamin K-dependent coagulation factors and the phenotype of the warfarin embryopathy: Clues to the mechanism of teratogenicity of coumarin derivatives
7. Hereditary deficiency of vitamin K-dependent coagulation factors with skeletal abnormalities
8. Cloning and expression of the cDNA for human γ-glutamyl carboxylase
9. Genomic sequence and transcription start site for the human γ-glutamyl carboxylase
10. A missense mutation in γ-glutamyl carboxylase gene causes combined deficiency of all vitamin K-dependent blood coagulation factors
11. Expression and characterization of the naturally occurring mutation L394R in human γ-glutamyl carboxylase
12. A novel mutation in the carboxylase gene resulting in congenital combined deficiency of vitamin K-dependent blood coagulation factors
13. Congenital deficiency of vitamin K-dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complex
14. The generation of mice genetically deficient in γ-carboxylase by gene targeting
15. Cloning or rat vitamin K-dependent gamma-glutamyl carboxylase and developmentally regulated gene expression in postimplantation embryos
16. Congenital deficiency of all vitamin K-dependent blood coagulation factors due to a defective vitamin K-dependent carboxylase in Devon Rex cats
17. Hereditary deficiency of vitamin K-dependent coagulation factors in Rambouillet sheep