A new G-6-PD variant associated with chronic non-spherocytic haemolytic anaemia in a negro family.
作者信息
Howell E B, Nelson A J, Jones O W
出版信息
J Med Genet. 1972 Jun;9(2):160-4. doi: 10.1136/jmg.9.2.160.
Abstract
摘要
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A new G-6-PD variant associated with chronic non-spherocytic haemolytic anaemia in a negro family.在一个黑人家庭中发现一种与慢性非球形红细胞溶血性贫血相关的新型葡萄糖-6-磷酸脱氢酶（G-6-PD）变异体。
J Med Genet. 1972 Jun;9(2):160-4. doi: 10.1136/jmg.9.2.160.
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"CHICAGO I" VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN CONGENITAL HEMOLYTIC DISEASE.先天性溶血性疾病中葡萄糖-6-磷酸脱氢酶的“芝加哥I”变体
J Lab Clin Med. 1964 May;63:715-25.
2
Improved method for the determination of blood glutathione.测定血液中谷胱甘肽的改进方法。
J Lab Clin Med. 1963 May;61:882-8.
3
Congenital nonspherocytic hemolytic anemia.先天性非球形细胞溶血性贫血
Am J Dis Child. 1961 Sep;102:313-20. doi: 10.1001/archpedi.1961.02080010315006.
4
The hemolytic effect of primaquine and related compounds: a review.伯氨喹及相关化合物的溶血作用：综述
Blood. 1959 Feb;14(2):103-39.
5
A deficiency of glucose-6-phosphate dehydrogenase activity in erythrocytes from patients with favism.蚕豆病患者红细胞中葡萄糖-6-磷酸脱氢酶活性缺乏。
Bull Johns Hopkins Hosp. 1958 Apr;102(4):169-75.
6
Hereditary hemolytic anemia with hexokinase deficiency. Role of hexokinase in erythrocyte aging.伴有己糖激酶缺乏的遗传性溶血性贫血。己糖激酶在红细胞衰老中的作用。
N Engl J Med. 1967 Jan 5;276(1):1-11. doi: 10.1056/NEJM196701052760101.
7
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Anemia, cataracts, and seizures in patient with glucose-6-phosphate dehydrogenase deficiency.葡萄糖-6-磷酸脱氢酶缺乏症患者的贫血、白内障和癫痫发作。
Arch Intern Med. 1966 Oct;118(4):385-90.
9
Evidence for four types of erythrocyte glucose-6-phosphate dehydrogenase from G-6-PD-deficient human subjects.来自葡萄糖-6-磷酸脱氢酶（G-6-PD）缺乏的人类受试者的四种红细胞葡萄糖-6-磷酸脱氢酶类型的证据。
J Clin Invest. 1966 Jun;45(6):823-31. doi: 10.1172/JCI105398.
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