目的：阐明海南汉族、黎族人群中葡萄糖-6-磷酸脱氢酶缺乏症的分子基础。
Objective:To elucidate the molecular basis of G6PD deficiency in the Han and Li nationalities in Hainan, China.
本文综述了近30余年来作者等对遗传性红细胞葡糖一6一磷酸脱氢酶缺乏症研究的概况。
Studies on glucose-6-phosphate dehydrogenase deficiency during the past 30 to 40 years are briefly reviewed.
方法用G6PD/6PGD比值法。 对7488例育龄人群进行了红细胞葡萄糖6-磷酸脱氢酶缺乏症临床检测。
Methods: Blood samples from 7488 persons at repreduction-age were examined on G6PD/6PGD hematology.
目的从红细胞膜蛋白磷酸化改变的角度探讨葡萄糖6磷酸脱氢酶(G6PD)缺乏症溶血的机制。
Objective To explore the hemolytic mechanism of glucose 6 phosphate dehydrogenase (G6PD) deficient erythrocytes in the view of phosphorylation of membrane protein.
葡萄糖- 6 -磷酸脱氢酶(G6PD)缺乏症是最常见的遗传性酶病，主要由于G6PD基因突变所致。
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most frequent genetic enzymopathy, mainly caused by mutations of G6PD gene.
目的分析云南人群中葡萄糖6 磷酸脱氢酶（G6PD）缺乏症患者的基因突变类型及分布特点。
Objective To analyze the types and distribution of glucose-6-phosphate dehydrogenase(G6PD) gene mutations in Yunnan province.
目的分析云南人群中葡萄糖6 磷酸脱氢酶（G6PD）缺乏症患者的基因突变类型及分布特点。
Objective To analyze the types and distribution of glucose-6-phosphate dehydrogenase(G6PD) gene mutations in Yunnan province.
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