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 is very common among people of Southeast Asian , Northeast Indian , Sri Lankan and Bangladeshi descent.

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 at a slightly reduced rate and hence has the phenotype of a mild form of β thalassemia.

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 characterized by marked clinical variability, ranging from a mild and asymptomatic anaemia to a life-threatening disorder requiring transfusions from infancy.

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 severe. Hb E trait and Hb EE are mild disorders. The combination of Hb E and Hb S (Hb SE) results in a sickle cell disease syndrome similar to sickle β + thalassemia.

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 anemia, but the condition typically does not cause any symptoms. It is inherited in an autosomal recessive manner and is caused by a genetic change in the HBB gene.

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，表现为轻度不稳定，可能与血红蛋白四聚体单体之间的结合松散有关。

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 bodies. HbE is passed from parent to child in genes. Genes carry information about human characteristics such as eye colour, hair colour and haemoglobin.

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. HbE is one of the most common variant of normal hemoglobin. Hemoglobin …