Novel mutation in the γ-glutamyl carboxylase gene resulting in congenital combined deficiency of all vitamin K-dependent blood coagulation factors

Medicine & Life Sciences

• glutamyl carboxylase 100%
• Vitamin K Deficiency 89%
• Blood Coagulation Factors 66%
• Mutation 32%
• Codon 28%
• Genes 23%
• Vitamin K 1 21%
• Inheritance Patterns 18%
• Tryptophan 15%
• Missense Mutation 15%
• Hemostasis 14%
• Restriction Fragment Length Polymorphisms 14%
• Point Mutation 14%
• Serine 14%
• Exons 12%
• Parents 10%
• Amino Acids 10%

Chemical Compounds

• Blood Clotting Factor 78%
• Vitamin 59%
• Mutation 49%
• Serine 9%
• Tryptophan 9%
• Amino-Acid Residue 8%