Szelényi J G, Horányi M, Földi J, Hudacsek J, István L, Hollán S R
Hemoglobin. 1980;4(1):27-38. doi: 10.3109/03630268009042371.
A hemoglobin variant of slow electrophoretic mobility has been demonstrated in a Hungarian female patient. The abnormal component amounted to about 30% and proved to be a new hemoglobin variant, alpha 49 (CE7) Ser replaced by Arg, which has been named Hb Savaria.
在一名匈牙利女性患者中发现了一种电泳迁移率缓慢的血红蛋白变体。异常成分约占30%,经证实是一种新的血红蛋白变体,即α49(CE7)位的丝氨酸被精氨酸取代,该变体被命名为Hb萨瓦里亚。