Hemoglobin E (HbE) is an abnormal hemoglobin with a single point mutation in the β chain. At position 26 there is a change in the amino acid , from glutamic acid to lysine (E26K). …

Hemoglobin E (HbE) is an extremely common structural hemoglobin variant that occurs at high frequencies throughout many Asian countries. It is a β-hemoglobin variant, which is produced …

Haemoglobin E-beta thalassaemia (Hb E/β-thalassaemia) is the genotype responsible for approximately one-half of all severe beta-thalassaemia worldwide. The disorder is …

血红蛋白（Hb）E是全球第三普遍的血红蛋白（仅次于Hb A和Hb S）。 它主要见于东南亚人群中 ，但在中国人中较少见。 杂合子（Hb AE）患者无症状，纯合子血红蛋白E病患者通常有轻度 …

2007年1月1日 · Hemoglobin (Hb) E is one of the world’s most common and important mutations. It results in a heterogeneous group of disorders whose phenotype range from asymptomatic to …

Hemoglobin E (HbE) disease is a mild, inherited blood disorder characterized by an abnormal form of hemoglobin, called hemoglobin E. People with this condition may have very mild …

Homozygous hemoglobin E (Hb E) disease is a hemoglobinopathy that causes a mild hemolytic anemia, usually without splenomegaly. (See also Overview of Hemolytic Anemia.) Hemoglobin …

hbe是β2珠蛋白基因第26位密码子的gag→aag突变导致该位置错义突变 （谷氨酸被赖氨酸取代），产生的β链变异异常血红蛋白。 当这一异常血红蛋白与氧化物接触后，表现为轻度不稳 …

Haemoglobin E (HbE) is a common inherited condition caused by the production of an abnormal haemoglobin protein. Haemoglobin is a protein in the blood that carries oxygen around our …

Hemoglobin E or haemoglobin E (HbE) is an abnormal hemoglobin with a single point mutation in the β chain. At position 26 there is a change in the amino acid, from glutamic acid to lysine. …