Dibenedetto S P, Russo Mancuso G, Di Cataldo A, Schilirò G
Cattedra di Ematologia Pediatrica, Università di Catania, Italy.
Haematologica. 1991 Sep-Oct;76(5):414-20.
A number of genetic or acquired conditions in which hemoglobin anomalies occur without detectable modifications of globin genes are reviewed. They include increased fetal hemoglobin (alpha 2 gamma 2), variations in hemoglobin A2 concentration, the presence of Hb H (beta 4), Bart's Hb (gamma 4), Hb Köelliker, glycosylated, carbamylated and acetylated hemoglobins.
本文综述了一些遗传或后天性疾病，这些疾病中血红蛋白异常出现，但珠蛋白基因未检测到修饰。它们包括胎儿血红蛋白（α2γ2）增加、血红蛋白A2浓度变化、Hb H（β4）、巴特血红蛋白（γ4）、科利克血红蛋白的存在、糖化、氨甲酰化和乙酰化血红蛋白。
