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Inherited thrombophilia genes in minorities
- Source :
- Genetic testing. 3(4)
- Publication Year :
- 2000
-
Abstract
- Mutations in several genes have recently been identified which predispose to thrombosis, specifically Factor V G1691A (Factor V Leiden), Prothrombin G20210A, and Methylene tetrahydrofolate redactase (MTHFR) C677T. The prevalence of these genes in European populations has been studied, but there is little data on their prevalence in minorities. Samples from a predominantly African-American population were analyzed for these mutations. While the G20210A mutation in the prothrombin gene and homozygosity for the C677T mutation of the MTHFR were not found in African-Americans, it appears that the carrier rate for the MTHFR C677T among Hispanics may be higher than in other reported groups.
- Subjects :
- China
Heterozygote
Population
Black People
medicine.disease_cause
Thrombophilia
White People
Asian People
Factor V Leiden
Medicine
Humans
Genetic Testing
education
Gene
Genetics (clinical)
Methylenetetrahydrofolate Reductase (NADPH2)
Genetics
Mutation
education.field_of_study
Oxidoreductases Acting on CH-NH Group Donors
biology
business.industry
Factor V
medicine.disease
digestive system diseases
United States
Methylenetetrahydrofolate reductase
biology.protein
Prothrombin G20210A
Prothrombin
business
Subjects
Details
- ISSN :
- 10906576
- Volume :
- 3
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Genetic testing
- Accession number :
- edsair.doi.dedup.....7d699fe024b0509c700dce8cc9b3649b