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 …

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) 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 trait is a condition that affects the red blood cells. Your red blood cells contain hemoglobin, which carries oxygen from the lungs to all parts of your body.

Hemoglobin E trait is an inherited blood disorder. That means it is passed down through your parent’s genes. It leads to an abnormal form of hemoglobin that may cause mild anemia. It …

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 …

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 …

Hemoglobin E trait is an inherited blood disorder. That means it's passed down through your parent’s genes. It leads to an abnormal form of hemoglobin that may cause mild anemia. It …

Hemoglobin is found in red blood cells and moves oxygen through the body. A person with hemoglobin E trait (Hb AE) has one copy of the gene that makes the usual hemoglobin (Hb A), …

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 …