<p>The data were collected from HbVar, the globin gene server <a href="http://globin.cse.psu.edu/globin/hbvar/" target="_blank">(http://globin.cse.psu.edu/globin/hbvar/</a>).</p><p>These different mutations led to an α-thalassemic phenotype more or less pronounced.</p><p>*the production of α-globin is under the control of two genes α1 and α2-globin genes (<i>HBA1</i> and <i>HBA2</i> respectively)</p><p>**Length expressed as number of amino-acid residues;</p><p>del, deletion; ins, insertion;</p><p>Natural variants in the G and H helices and C terminal extremity altering the sequence length of α-Hb.</p
Objectives: Alpha (α) and beta (β) thalassemia are the most prevalent genetic hematological disorder...
Single amino acid substitutions in the globin chain are the most common forms of genetic variations ...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
The human α-globin genes are paralogues, sharing a high degree of DNA sequence similarity and produc...
International audienceA small group of hemoglobin (Hb) variants result from 'in-frame' deletion/inse...
textabstractThe human α-globin genes are paralogues, sharing a high degree of DNA sequence similarit...
Hemoglobin (Hb) is a protein responsible for oxygen transportation from lungs to the entire body. It...
A number of deletions have been documented among the non-α globin genes of man that are associated w...
Haemoglobin variants in which a frameshift results in chain elongation are unusual. Haemoglobin Cran...
Introduction: Interactions of different hemoglobin variants with thalassemia alleles can result in ...
The major component of the red blood cells is hemoglobin A which consists of 2α- and 2β-globin chain...
The human α-globin gene complex on chromosome 16 consists of two adult α genes (α1 and α2) separated...
Over the past three decades, a vast amount of new information has been uncovered describing how the ...
International audienceWe report three cases with very heterogeneous Hb A(2) levels caused by known c...
<p>The most common ones among today’s inhabitants of the northern part of the Indian subcontinent we...
Objectives: Alpha (α) and beta (β) thalassemia are the most prevalent genetic hematological disorder...
Single amino acid substitutions in the globin chain are the most common forms of genetic variations ...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
The human α-globin genes are paralogues, sharing a high degree of DNA sequence similarity and produc...
International audienceA small group of hemoglobin (Hb) variants result from 'in-frame' deletion/inse...
textabstractThe human α-globin genes are paralogues, sharing a high degree of DNA sequence similarit...
Hemoglobin (Hb) is a protein responsible for oxygen transportation from lungs to the entire body. It...
A number of deletions have been documented among the non-α globin genes of man that are associated w...
Haemoglobin variants in which a frameshift results in chain elongation are unusual. Haemoglobin Cran...
Introduction: Interactions of different hemoglobin variants with thalassemia alleles can result in ...
The major component of the red blood cells is hemoglobin A which consists of 2α- and 2β-globin chain...
The human α-globin gene complex on chromosome 16 consists of two adult α genes (α1 and α2) separated...
Over the past three decades, a vast amount of new information has been uncovered describing how the ...
International audienceWe report three cases with very heterogeneous Hb A(2) levels caused by known c...
<p>The most common ones among today’s inhabitants of the northern part of the Indian subcontinent we...
Objectives: Alpha (α) and beta (β) thalassemia are the most prevalent genetic hematological disorder...
Single amino acid substitutions in the globin chain are the most common forms of genetic variations ...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...