Kazazian H H, Dowling C E, Waber P G, Huang S, Lo W H
Blood. 1986 Oct;68(4):964-6.
To make possible prenatal diagnosis of beta-thalassemia in China and Southeast Asia by direct detection of mutant beta-globin genes, we have determined the spectrum of mutations producing the disorder in this region of the world. Seventy-eight beta-thalassemia genes from Chinese and Southeast Asians were randomly obtained, and the relevant mutation was characterized in 76 (98%) of them. Seven different point mutations were found among the 78 genes studied. Of these seven beta-thalassemia alleles, two constitute 62%, and two others account for 29% of the total. Since only four alleles make up 91% of the mutant genes, prenatal diagnosis of beta-thalassemia in China and Southeast Asia should be feasible by simplified techniques for direct detection of point mutations.
为了通过直接检测β-珠蛋白基因突变实现中国和东南亚地区β地中海贫血的产前诊断,我们确定了世界该地区导致该疾病的突变谱。随机获取了来自中国和东南亚人的78个β地中海贫血基因,其中76个(98%)的相关突变得到了鉴定。在所研究的78个基因中发现了7种不同的点突变。在这7个β地中海贫血等位基因中,两个占总数的62%,另外两个占29%。由于仅4个等位基因就构成了91%的突变基因,因此通过简化的点突变直接检测技术,在中国和东南亚进行β地中海贫血的产前诊断应该是可行的。