The molecular basis of α-thalassemias: Frequent occurrence of dysfunctional α loci among non-Asians with Hb H disease-Reference-Cited by-同舟云学术

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The molecular basis of α-thalassemias: Frequent occurrence of dysfunctional α loci among non-Asians with Hb H disease

Published:1979-05 Issue:1 Volume:17 Page:33-42
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Orkin Stuart H.,Old John,Lazarus Herbert,Altay Cigdem,Gurgey Aytemiz,Weatherall David J.,Nathan David G.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference39 articles.

1. Alpha-thalassemia

2. The thalassemia syndromes

3. Globin Messenger RNA in Hemoglobin H Disease

4. Haemoglobin Constant Spring—A Chain Termination Mutant ?

5. A very large repeating unit of mouse DNA containing the 18S, 28S and 5.8S rRNA genes

Cited by 165 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. Alpha-Thalassemia Carrier due to –α3.7 Deletion: Not So Silent;Acta Haematologica;2020

2. The Hemoglobinopathies: An Empowering Era of Human Genetics in the Clinic and the Laboratory;The FASEB Journal;2017-08-15

3. Molecular diagnosis of α-thalassemia in a multiethnic population;European Journal of Haematology;2017-04-06

4. Hemoglobin H Disease in Turkey: Experience from Eight Centers;Turkish Journal of Hematology;2016-02-19

5. A Journey in Science: Early Lessons from the Hemoglobin Field;Molecular Medicine;2014-01

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