西班牙一家族中葡萄糖-6-磷酸脱氢酶慢变体型伴缺乏症。与Gd（阴性）西雅图变体型的关系。 - Suppr

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超能文献

Glucose-6-phosphate dehydrogenase slow variant with deficiency in a Spanish family. Relationship with the Gd (minus) Seattle variant.

作者信息

Kahn A, Vives-Corrons J L, Cottreau D, Boivin P

出版信息

Biomedicine. 1974 Jul;21(7):303-7.

PMID:4433664

Abstract

摘要

相似文献

Glucose-6-phosphate dehydrogenase slow variant with deficiency in a Spanish family. Relationship with the Gd (minus) Seattle variant.西班牙一家族中葡萄糖-6-磷酸脱氢酶慢变体型伴缺乏症。与Gd（阴性）西雅图变体型的关系。

Biomedicine. 1974 Jul;21(7):303-7.

[Congenital deficiency in glucose-6-phosphate dehydrogenase. Slow variant found in a Spanish family. Relation with the variant Gd(minus) "Seattle" (author's transl)].

Sangre (Barc). 1974;19(4):435-42.

[Deficiency of red cell glucose-6-phosphate-dehydrogenase due to a slow variant in a French family. Relationship with the Gd (-) Seattle variant (author's transl)].[一个法国家庭中因慢变体型导致的红细胞葡萄糖-6-磷酸脱氢酶缺乏症。与Gd(-)西雅图变体型的关系（作者译）]

Nouv Rev Fr Hematol. 1973 Mar-Apr;13(2):163-71.

[Glucose-6-phosphate dehydrogenase type Schwaben. A new enzyme variant with spontaneous hemolytic anemia].施瓦本型葡萄糖-6-磷酸脱氢酶。一种伴有自发性溶血性贫血的新型酶变体

Dtsch Med Wochenschr. 1971 Jun 11;96(24):1029-33. doi: 10.1055/s-0028-1108377.

[Electrophoretic and kinetic properties of erythrocyte glucose-6-phosphate dehydrogenase (Gd) in hereditary enzyme deficiency. A new variant of glucose-6-phosphate dehydrogenase : Gd Kremenchug].遗传性酶缺乏症中红细胞葡萄糖-6-磷酸脱氢酶（Gd）的电泳和动力学特性。葡萄糖-6-磷酸脱氢酶的一种新变体：Gd 克雷门丘格

Nouv Rev Fr Hematol (1978). 1978;20(4):557-64.

Characterization of erythrocytic glucose-6-phosphate dehydrogenase in a mouse strain with reduced G6PD activity.葡萄糖-6-磷酸脱氢酶活性降低的小鼠品系中红细胞葡萄糖-6-磷酸脱氢酶的特性分析

Biomed Biochim Acta. 1991;50(3):233-8.

[Detection of a new anomalous variant of glucose-6-phosphate dehydrogenase in human erythrocytes].[人红细胞中葡萄糖-6-磷酸脱氢酶一种新的异常变体的检测]

Biull Eksp Biol Med. 1977 Dec;84(12):728-31.

Characteristics of a new abnormal variant of G-6-PD in human red cells.人类红细胞中葡萄糖-6-磷酸脱氢酶（G-6-PD）一种新的异常变体的特征

Acta Biol Med Ger. 1977;36(5-6):753-8.

[Federal District glucose-6-phosphate dehydrogenase Gd(-). A new variant associated with moderate enzyme deficiency and occasional hemolytic anemia].[联邦区葡萄糖-6-磷酸脱氢酶Gd(-)。一种与中度酶缺乏和偶发性溶血性贫血相关的新变体]

Rev Invest Clin. 1981 Apr-Jun;33(2):209-11.

[Description of new mutant forms of erythrocyte glucose-6-phosphate dehydrogenase in man].[人类红细胞葡萄糖-6-磷酸脱氢酶新突变形式的描述]

Genetika. 1975;11(12):116-22.

引用本文的文献

Hereditary erythrocyte pyruvate-kinase (PK) deficiency and chronic hemolytic anemia: clinical, genetic and molecular studies in six new Spanish patients.遗传性红细胞丙酮酸激酶（PK）缺乏症与慢性溶血性贫血：对6名西班牙新患者的临床、遗传及分子研究

Hum Genet. 1980;53(3):401-8. doi: 10.1007/BF00287063.

Molecular mechanism of glucose-6-phosphate dehydrogenase deficiency.葡萄糖-6-磷酸脱氢酶缺乏症的分子机制。

Humangenetik. 1974;25(2):101-9. doi: 10.1007/BF00283310.

GD (--) Aachen, a new variant of deficient glucose-6-phosphate dehydrogenase. Clinical, genetic, biochemical aspects.GD（--）亚琛型，葡萄糖-6-磷酸脱氢酶缺乏的一种新变体。临床、遗传、生化方面。

Hum Genet. 1976 May 19;32(2):171-80. doi: 10.1007/BF00291500.

G-6PD "ankara". a new G-6PD variant with deficiency found in a Turkish family.

Humangenetik. 1975;27(3):247-50. doi: 10.1007/BF00278353.

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