Alberti R, Mariuzzi G M, Marinucci M, Bruni E, Tenteri L
J Med Genet. 1975 Sep;12(3):294-6. doi: 10.1136/jmg.12.3.294.
A survey of haemoglobin variants undertakin in an Italian community (Polesine) has revealed the presence of haemoglobin Hasharon (alpha2 47 Asp yields His beta2) in 108 subjects from 40 families. The variant accounted for 30 to 40% of the total haemoglobin. In subjects doubly heterozygous for Hb Hasharon and beta thalassaemia, the proportion was 17 to 19%. Though there was some evidence that the variant was unstable in vitro, there was no obvious haemoglobinopathy in vivo.
在意大利一个社区(波莱西内)开展的一项血红蛋白变体调查显示,在来自40个家庭的108名受试者中存在血红蛋白哈沙龙(α2 47天冬氨酸变为组氨酸β2)。该变体占总血红蛋白的30%至40%。在血红蛋白哈沙龙和β地中海贫血的双重杂合子受试者中,这一比例为17%至19%。尽管有一些证据表明该变体在体外不稳定,但在体内没有明显的血红蛋白病。