THE MOLECULAR-BASIS OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY

被引:98
|
作者
VULLIAMY, T
MASON, P
LUZZATTO, L
机构
[1] Department of Haematology, Royal Postgraduate Medical School, Hammersmith Hospital, London, W12 0NN, Ducane Road
关键词
D O I
10.1016/0168-9525(92)90372-B
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
With more than 300 different variants reported, the human enzyme glucose-6-phosphate dehydrogenase (G6PD; EC 1.1.1.49) is one of the most polymorphic proteins known. An estimated 400 million people throughout the world are deficient in G6PD; numerous lines of evidence indicate that this is because female heterozygotes have a selective advantage in malaria infections. The cloning of the G6PD gene has made it possible to clarify the molecular basis underlying this enzyme deficiency and polymorphism.
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页码:138 / 143
页数:6
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