Romain P L, Schwartz A D, Shamsuddin M, Adams J G, Mason R G, Vida L N, Honig G R
Blood. 1975 Mar;45(3):387-93.
An electrophoretically fast-moving hemoglobin variant was found in a 2-yr-old boy who was referred for evaluation with findings of iron deficiency anemia. The anemia was corrected, and no hematologic abnormality remained after treatment with iron. Oxygen affinity of the blood was normal, and no evidence was found of instability of the variant hemoglobin. Structural studies demonstrated a substitution of aspartic acid for alanine at beta76 (E20). This change did not appear to cause any functional disruption of the hemoglobin in this patient, as would be predicted by the position of the affected animo acid residue on the surface of the molecule.
在一名因缺铁性贫血被转诊评估的2岁男孩中发现了一种电泳快速移动的血红蛋白变体。贫血得到纠正,铁治疗后未遗留血液学异常。血液的氧亲和力正常,未发现该变体血红蛋白不稳定的证据。结构研究表明,β76(E20)位的丙氨酸被天冬氨酸替代。正如受影响氨基酸残基在分子表面的位置所预测的那样,这种变化似乎并未导致该患者血红蛋白的任何功能破坏。