Glucose-6-phosphate dehydrogenase (G6PD) mutations in Myanmar: G6PD Mahidol (487G>A) is the most common variant in the Myanmar population
β Scribed by Hiroyuki Matsuoka; Jichun Wang; Makoto Hirai; Meiji Arai; Shigeto Yoshida; Tamaki Kobayashi; Amadu Jalloh; Khin Lin; Fumihiko Kawamoto
- Publisher
- Nature Publishing Group
- Year
- 2004
- Tongue
- English
- Weight
- 214 KB
- Volume
- 49
- Category
- Article
- ISSN
- 1435-232X
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π SIMILAR VOLUMES
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%
Glucose-6-phosphate dehydrogenase (G6PD) deficiency has previously been reported among both the black and white populations of Costa Rica. All 28 G6PD A-samples were found to be of the common G6PD A--376G/2~ A previously described mutation associated with nonspherocytic hemolytic anemia, G6PD Puert