Compound heterozygosity for one novel and one recurrent mutation in a Thai patient with severe protein S deficiency. [electronic resource]
Producer: 19990604Description: 189-92 p. digitalISSN:- 0340-6245
- Alleles
- Blindness -- etiology
- Codon -- genetics
- DNA Mutational Analysis
- Disseminated Intravascular Coagulation -- etiology
- Endophthalmitis -- etiology
- Exons -- genetics
- Female
- Fetal Diseases -- etiology
- Gene Frequency
- Genetic Predisposition to Disease
- Heterozygote
- Humans
- IgA Vasculitis -- congenital
- Infant, Newborn
- Point Mutation
- Protein S -- genetics
- Protein S Deficiency -- complications
- Retinal Vein Occlusion -- embryology
- Risk Factors
- Thailand
- Thrombophilia -- epidemiology
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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