Article
Glucose-6-phosphate dehydrogenase (G6PD) mutations in Thailand: G6PD Viangchan (871G>A) is the most common deficiency variant in the Thai population.
Human mutation - 1 Feb 2002
Nuchprayoon I, Sanpavat S, Nuchprayoon S
Abstract excerpt
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common hereditary disorder in humans. Through a population study for G6PD deficiency using a cord blood quantitative G6PD assay in Bangkok, Thailand, we found that the prevalence of G6PD deficiency is 11.1% in Thai male (N=350) and 5.8% in female (N=172) cord blood samples. Among the neonates with hyperbilirubinemia, the prevalence of G6PD deficiency...
Topics
- Asian People
- DNA Mutational Analysis
- Female
- Gene Frequency
- Genetic Testing
- Glucosephosphate Dehydrogenase
- Humans
- Infant, Newborn
- Jaundice, Neonatal
- Male
- Metabolism, Inborn Errors
- Mutation
- Polymerase Chain Reaction
- Thailand
