Polymorphism of red cell glyoxalase I (E.C.: 4.4.1.5). A new genetic marker in man
作者： J. Kömpf , S. Gussmann , S. Bissbort , H. Ritter
DOI: 10.1007/BF00273329
关键词:
摘要: The polymorphism of glyoxalase I was investigated in 169 mother-child combinations from southwestern Germany. Glyoxalase (GLO) has 3 common phenotypes: GLO 1, 2-1, and 2. results are good agreement with the formal hypothesis: Two alleles GLO1 GLO2 at an autosomal locus. gene frequency estimated to be 0.39. From electrophoretic pattern GLO-molecule appears consist two subunits.
springer.com
sci-hub.se 参考文章(2)
S. Bissbort, J. Kömpf, Population genetics of red cell galactose-1-phosphate-uridyl-transferase (EC: 2.7.7.12) Human Genetics. ,vol. 17, pp. 79- 80 ,(1972) , 10.1007/BF01789605
Eva K. Sober, Philip P. Cohen, Glyoxalase Activity of Erythrocytes from Cancerous Rats and Human Subjects Cancer Research. ,vol. 5, pp. 631- 632 ,(1945)