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β-半乳糖苷酶缺乏症:对两名长期存活患者的研究。

Beta-galactosidase deficiency: studies of two patients with prolonged survival.

作者信息

Taylor H A, Stevenson R E, Parks S E

出版信息

Am J Med Genet. 1980;5(3):235-45. doi: 10.1002/ajmg.1320050304.

Abstract

Two adults with beta-galactosidase deficiency were studied. Differences in a number of beta-galactosidase parameters (pH optima, heat denaturation, NaCl kinetics) were noted between the patients. Differences were also noted in beta-galactosidase electrophoretic mobilities and urinary oligosaccharides; however, there was no complementation in cell fusion studies. It is suggested that these two patients have different primary mutations at the beta-galactosidase locus which are probably structural in nature.

摘要

对两名患有β-半乳糖苷酶缺乏症的成年人进行了研究。在患者之间发现了一些β-半乳糖苷酶参数(最适pH值、热变性、NaCl动力学)的差异。在β-半乳糖苷酶电泳迁移率和尿寡糖方面也发现了差异;然而,细胞融合研究中没有互补现象。提示这两名患者在β-半乳糖苷酶基因座存在不同的原发性突变,这些突变可能本质上是结构性的。

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