Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficient newborn with massive thrombosis. [electronic resource]
Producer: 19960912Description: 877-80 p. digitalISSN:- 0006-4971
- Adult
- Base Sequence
- Consanguinity
- Disease Susceptibility
- Factor V -- genetics
- Factor V Deficiency -- genetics
- Female
- Genetic Heterogeneity
- Heterozygote
- Humans
- Infant, Newborn
- Male
- Middle Aged
- Molecular Sequence Data
- Pedigree
- Protein C -- genetics
- Thrombophlebitis -- genetics
- Thrombosis -- congenital
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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