Novel splice site mutations in the gamma glutamyl carboxylase gene in a child with congenital combined deficiency of the vitamin K-dependent coagulation factors (VKCFD). [electronic resource]
Producer: 20090602Description: 92-5 p. digitalISSN:- 1545-5017
- Blood Coagulation Factors -- genetics
- Carbon-Carbon Ligases -- deficiency
- Child
- Coagulation Protein Disorders -- congenital
- Diagnosis, Differential
- Humans
- Male
- Mixed Function Oxygenases -- genetics
- Munchausen Syndrome -- diagnosis
- Mutation
- Polymorphism, Single Nucleotide
- Vitamin K -- administration & dosage
- Vitamin K Deficiency -- congenital
- Vitamin K Epoxide Reductases
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.