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一个同时患有半乳糖血症和杜阿尔特变异型的家族中红细胞半乳糖-1-磷酸尿苷酰转移酶的等电聚焦分析

Isoelectrofocusing of erythrocyte galactose 1 phospho uridyl transferase in a family with both galactosemia and Duarte variants.

作者信息

Schapira F, Gregori C, Banroques J, Vidailhet M, Despoisses S, Vigneron C

出版信息

Hum Genet. 1979 Jan 19;46(1):89-96. doi: 10.1007/BF00278906.

Abstract

A family with the presence of the genes for both galactosemia and the Duarte variant is described. Galactose 1 phospho uridyl transferase has been studied not only by electrophoresis on starch gel, but also by isoelectro-focusing on thin-layer acrylamide. Normal and variant transferases were resolved into three bands, the isoelectric point of which was between 5.40 and 5.10 for the normal subjects, and between 5.25 and 4.95 for subjects with the Duarte variant.

摘要

本文描述了一个同时存在半乳糖血症基因和杜阿尔特变异基因的家族。不仅通过淀粉凝胶电泳,还通过薄层丙烯酰胺等电聚焦法对1-磷酸半乳糖尿苷转移酶进行了研究。正常和变异转移酶被分离为三条带,正常受试者的等电点在5.40至5.10之间,杜阿尔特变异受试者的等电点在5.25至4.95之间。

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