Vergnes H, Brun H
Hum Genet. 1979;53(1):43-5. doi: 10.1007/BF00289449.
The existence of a microheterogeneity of glucose-6-phosphate dehydrogenase (G6PD) in human erythrocyte lysates has been previously demonstrated using isoelectric focusing (Der Kaloustian et al., 1974; Turner et al., 1975). The application of this method, modified in some aspects, to the identification of various G6PD variants led to interesting conclusions. The results reported here have been obtained from a study of four distinct molecular types: Gd(-) Mediterranean, Gd(-) Kabyle, the African Gd(+) A, and a new almost undescribed G6PD variant with severe enzyme deficiency named Gd(-) Muret.
先前已通过等电聚焦证明人红细胞裂解物中存在葡萄糖-6-磷酸脱氢酶(G6PD)的微异质性(Der Kaloustian等人,1974年;Turner等人,1975年)。将该方法在某些方面进行改进后应用于鉴定各种G6PD变体,得出了有趣的结论。此处报告的结果来自对四种不同分子类型的研究:Gd(-)地中海型、Gd(-)卡拜尔型、非洲Gd(+) A型,以及一种几乎未被描述过的具有严重酶缺陷的新型G6PD变体,名为Gd(-) 米雷型。