Globin biosynthesis in sickle cell, Hb SC, and Hb C diseases
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference34 articles.
1. Globin synthesis in clinically significant disorders with Hb S or Hb C;Kim;Pediatr Res,1975
2. The synthesis of abnormal haemoglobins;White;Biochimie,1972
3. The synthesis of globin peptide chains in sickle-cell disease;Sarup;Br J Haematol,1974
4. Preferential binding of βS globin chains associated with stroma in sickle cell disorders;Bank;J Clin Invest,1974
5. Clinical, hematologic and biosynthetic studies in sickle cell-βo-thalassemia: A comparison with sickle cell anemia;Steinberg;Am J Hematol,1976
Cited by 4 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. The Clinical Significance of Breastmilk Maturation Rates;Birth;1987-12
2. Molecular analysis of the beta-thalassemia phenotype associated with inheritance of hemoglobin E (alpha 2 beta2(26)Glu leads to Lys).;Journal of Clinical Investigation;1981-07-01
3. Inclusions in Red Blood Cells Containing Hb S or Hb C;British Journal of Haematology;1980-04
4. Modification of Hemoglobin H Disease by Sickle Trait;Journal of Clinical Investigation;1979-10-01
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