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关于人类红细胞NADH黄递酶遗传决定的电泳变异体的发生率及分离的进一步数据。

Further data on the incidence and segregation of genetically determined electrophoretic variants of human red cell NADH diaphorase.

作者信息

Williams L, Hopkinson D A

出版信息

Hum Hered. 1975;25(3):161-71. doi: 10.1159/000152723.

Abstract

Human red cell NADH diaphorase isozyme patterns have been examined in 3,060 unrelated Australians of European origin, by starch gel electrophoresis. 26 people with variant isozyme patterns were encountered: 12 were phenotype Dia 2-1 and 13 were Dia 4-1. A new variant isozyme pattern (Dia 7-1) was identified. No variants were identified in 100 Melanesians and 70 Australian Aborigines.

摘要

通过淀粉凝胶电泳法,对3060名无血缘关系的欧洲裔澳大利亚人进行了人类红细胞NADH黄递酶同工酶谱检测。发现26人具有变异同工酶谱:12人为Dia 2-1表型,13人为Dia 4-1表型。鉴定出一种新的变异同工酶谱(Dia 7-1)。在100名美拉尼西亚人和70名澳大利亚原住民中未发现变异情况。

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