Flatz G, Wilke K, Syagailo Y V, Eigel A, Horst J
Human Genetics, Medizinische Hochschule, Hannover, Germany.
Hum Mutat. 1999;13(3):258. doi: 10.1002/(sici)1098-1004(1999)13:3<258::aid-humu16>3.0.co;2-4.
The beta-thalassemia mutations of 13 unrelated heterozygous Germans who remained unidentified in a previous study of 40 subjects were investigated at the DNA level. Two Mediterranean, one Asian and three novel mutations (CD6 -G, CDs 108 /112-12nt, CDs 130/131 + GCCT) were identified. Altogether, in 30 of the 35 subjects (86%) in which a mutation in the beta-globin gene was identified, the mutation was of Mediterranean origin. The geographical distribution suggests recent migration from the Mediterranean region as cause of the high proportion of frequent Mediterranean beta-thalassemia mutations in the German population. Our results support the notion that the majority of beta-thalassemia genes in the western and central European population are of Mediterranean origin.
在一项对40名受试者的前期研究中仍未明确的13名无亲缘关系的德国杂合子β地中海贫血突变,在DNA水平上进行了调查。鉴定出了两种地中海型、一种亚洲型和三种新突变(CD6 -G、CDs 108/112-12nt、CDs 130/131 + GCCT)。在总共35名鉴定出β珠蛋白基因突变的受试者中,有30名(86%)的突变源自地中海地区。地理分布表明,近期来自地中海地区的移民是德国人群中常见的地中海型β地中海贫血突变比例较高的原因。我们的结果支持这样一种观点,即西欧和中欧人群中的大多数β地中海贫血基因源自地中海地区。