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与无症状性高酶缺乏相关的葡萄糖-6-磷酸脱氢酶基因新型错义突变的描述

Description of a novel missense mutation of glucose-6-phosphate dehydrogenase gene associated with asymptomatic high enzyme deficiency.

作者信息

Minucci Angelo, Concolino Paola, Antenucci Mirca, Santonocito Concetta, Ameglio Franco, Zuppi Cecilia, Giardina Bruno, Capoluongo Ettore

机构信息

Laboratory of Clinical Molecular Biology, Department of Biochemistry and Clinical Biochemistry, Catholic University, Largo F Vito 1, 00168, Rome, Italy.

出版信息

Clin Biochem. 2007 Aug;40(12):856-8. doi: 10.1016/j.clinbiochem.2007.03.025. Epub 2007 Apr 20.

Abstract

We report a case of an asymptomatic young subject affected by severe deficiency of Glucose 6-phosphate dehydrogenase (G6PD) activity. A novel genetic mutation (G130A) in the third exon was found. We named this novel mutation the "G6PD RIGNANO variant". These findings may contribute to a better knowledge of molecular epidemiology of the G6PD mutation and may represent an additional variant to be studied for a deep comprehension of in vivo compensation mechanisms of G6PD deficiency.

摘要

我们报告了一例葡萄糖-6-磷酸脱氢酶(G6PD)活性严重缺乏的无症状年轻患者。在第三个外显子中发现了一种新的基因突变(G130A)。我们将这种新突变命名为“G6PD里尼亚诺变体”。这些发现可能有助于更好地了解G6PD突变的分子流行病学,并且可能代表一种有待研究的额外变体,以深入理解G6PD缺乏的体内补偿机制。

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