一名患有地中海贫血-血红蛋白-I病患者的红细胞镰状化。 - Suppr

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超能文献

Sickling of erythrocytes in a patient with thalassemia-hemoglobin-I disease.

作者信息

ATWATER J, SCHWARTZ I R, ERSLEV A J, MONTGOMERY T L, TOCANTINS L M

出版信息

N Engl J Med. 1960 Dec 15;263:1215-23. doi: 10.1056/NEJM196012152632402.

DOI:10.1056/NEJM196012152632402

PMID:13685016

Abstract

摘要

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Sickling of erythrocytes in a patient with thalassemia-hemoglobin-I disease.一名患有地中海贫血-血红蛋白-I病患者的红细胞镰状化。

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引用本文的文献

Thalassaemia.地中海贫血

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Further studies on the isolation and properties of alpha-chain sub-units of haemoglobin.进一步研究血红蛋白 α-链亚单位的分离和性质。

Biochem J. 1966 Dec;101(3):843-51. doi: 10.1042/bj1010843.

BETA THALASSEMIA-HEMOGLOBIN D ALPHA. A FAMILY REPORT.β地中海贫血-血红蛋白Dα。一份家族报告。

Am J Hum Genet. 1965 Mar;17(2):148-55.

THE COEXISTENCE OF THE GENES FOR HEMOGLOBIN E AND ALPHA-THALASSEMIA IN THAIS, WITH RESULTANT SUPPRESSION OF HEMOGLOBIN E SYNTHESIS.血红蛋白E基因与α地中海贫血基因在泰国人中的共存，导致血红蛋白E合成受到抑制。

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Hb alpha 2glu beta 2 (Hb I) in a Caucasian family: independent mutation of common origin?一个高加索家庭中的血红蛋白α2谷氨酸β2（Hb I）：共同起源的独立突变？

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Diminished synthesis of an alpha chain mutant, hemoglobin I (alpha-16 lys leads to glu).α链突变体血红蛋白I（α-16赖氨酸突变为谷氨酸）的合成减少。

J Clin Invest. 1970 Dec;49(12):2218-21. doi: 10.1172/JCI106440.

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