Decrease of Alpha-Hasharon Globin in Beta-Thalassaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1978.tb03622.x/fullpdf
Reference14 articles.
1. Haemoglobin Hasharon in a north Italian community.
2. Absence of beta Globin Synthesis and Excess of alpha Globin Synthesis in Homozygous beta-Thalassemia
3. Excess of alpha-Globin Synthesis in Homozygous beta-Thalassemia and its Removal from the Red Blood Cell Cytoplasm
4. Kinetic Evidence for the Existence of alpha-Globin Pool in beta-Thalassemic Reticulocytes
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Organization of α-Globin Genes and mRNA Translation in Subjects Carrying Haemoglobin Hasharon (α47 Asp → His) from the Ferrara Region (Northern Italy);European Journal of Biochemistry;2005-03-03
2. Thalassaemia intermedia in a family with beta 0-thalassaemia and Hb Hasharon.;Journal of Medical Genetics;1982-12-01
3. Molecular Characteristics of a Non-deletion alpha-Thalassaemia of the Po River Delta;European Journal of Biochemistry;1981-05
4. Post-translational control of human hemoglobin synthesis The role of the differential affinity between globin chains in the control of mutated globin gene expression;Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis;1980-12
5. Hemoglobin Hasharon [α2 47 (CD5) Asp→ His β2]Linked to α-Thalassemia in Northern Italian Carriers;Acta Haematologica;1980
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