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

被引:15
|
作者
Minucci, Angelo [1 ]
Concolino, Paola [1 ]
Antenucci, Mirca [1 ]
Santonocito, Concetta [1 ]
Ameglio, Franco [1 ]
Zuppi, Cecilia [1 ]
Giardina, Bruno [1 ]
Capoluongo, Ettore [1 ]
机构
[1] Univ Cattolica Sacro Cuore, Lab Clin Mol Biol, Dept Biochem & Clin Biochem, I-00168 Rome, Italy
关键词
favism; G130A mutation; G6PD Rignano; Ala44Thr;
D O I
10.1016/j.clinbiochem.2007.03.025
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
We report a case of an asymptomatic young subject affected by severe deficiency of Glucose 6-phosphate debydrogenase (GOD) 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. (c) 2007 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:856 / 858
页数:3
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