Add to ORKGHemoglobin E is a slow moving B chain variant of hemoglobin, first discovered by Itano1. Characterized by Hunt et al2 showed glutamic acid at B 26 to be replaced by lysine. It is a common variant of hemoglobin in the world and reported in high frequency from South-East Asia3-6. Cases of Hb E, in combination with thalassemia have been reported on the basis of electrophoretic pattern only. In this communication a case of Hb E with B thalassemia is reported on the basis of amino acid sequencing of the abnormal peptide
Background: HbQ-India is a rare alpha chain variant. It is an important member of the hemoglobin Q f...
The distribution of hemoglobin E (α2β2 26Glu ®Lys ) is mostly restricted to Northea...
Abstract. Hemoglobin E (HbE) is one of the most prevalent β-globin variant, which is widely distribu...
Hemoglobin E is a slow moving B chain variant of hemoglobin, first discovered by Itano1. Characteriz...
Background:Hemoglobin E is an important hemoglobin variant with a worldwide distribution. A number o...
Hemoglobin E is probably the most common structural hemoglobin variant with thalassaemic properties ...
Haemoglobin (Hb) K Woolwich is a rare Hb variant which was first described in a family from West Ind...
Haemoglobin E (Hb E) is a variant of structurally abnormal haemoglobin that can be found very common...
Background: Hemoglobin E is an important hemoglobin variant with a worldwide distribution. A number ...
Background: Haemoglobinopathies are the commonest hereditary disorders in India and pose a major hea...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
HbDPunjab is an uncommon variant hemoglobin that does not result in significant pathology when inher...
Structural hemoglobin (Hb) variants typically are based on a point mutation in a globin gene that pr...
Abstract Background: Haemoglobinopathies are the commonest hereditary disorders in India and pose a ...
Hb Malay was first described in 1989 following an investigation of anaemia in a 22-year-old Malay ge...
Background: HbQ-India is a rare alpha chain variant. It is an important member of the hemoglobin Q f...
The distribution of hemoglobin E (α2β2 26Glu ®Lys ) is mostly restricted to Northea...
Abstract. Hemoglobin E (HbE) is one of the most prevalent β-globin variant, which is widely distribu...
Hemoglobin E is a slow moving B chain variant of hemoglobin, first discovered by Itano1. Characteriz...
Background:Hemoglobin E is an important hemoglobin variant with a worldwide distribution. A number o...
Hemoglobin E is probably the most common structural hemoglobin variant with thalassaemic properties ...
Haemoglobin (Hb) K Woolwich is a rare Hb variant which was first described in a family from West Ind...
Haemoglobin E (Hb E) is a variant of structurally abnormal haemoglobin that can be found very common...
Background: Hemoglobin E is an important hemoglobin variant with a worldwide distribution. A number ...
Background: Haemoglobinopathies are the commonest hereditary disorders in India and pose a major hea...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
HbDPunjab is an uncommon variant hemoglobin that does not result in significant pathology when inher...
Structural hemoglobin (Hb) variants typically are based on a point mutation in a globin gene that pr...
Abstract Background: Haemoglobinopathies are the commonest hereditary disorders in India and pose a ...
Hb Malay was first described in 1989 following an investigation of anaemia in a 22-year-old Malay ge...
Background: HbQ-India is a rare alpha chain variant. It is an important member of the hemoglobin Q f...
The distribution of hemoglobin E (α2β2 26Glu ®Lys ) is mostly restricted to Northea...
Abstract. Hemoglobin E (HbE) is one of the most prevalent β-globin variant, which is widely distribu...