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Title: Genetic polymorphism of human plasminogen. Author: Raum D, Marcus D, Alper CA. Journal: Am J Hum Genet; 1980 Sep; 32(5):681-9. PubMed ID: 7424908. Abstract: Using isoelectric focusing (IEF) in polyacrylamide gel of neuraminidase-treated serum or plasma samples and immunofixation or caseinolytic overlay after urokinase activation of gels, a common genetic polymorphism in human plasminogen has been delineated. Two alleles PLGN*A and PLGN*B, were observed with gene frequencies in whites of .69 and .30; in Orientals of .96 and .03; and in blacks of .80 and .18. Several rare alleles were also found. The distribution of phenotypes fits the Hardy-Weinberg equilibrium. Inheritance is autosomal codominant and fits the expectations of Mendelian inheritance. There is fetal synthesis, but no transplacental passage of plasminogen in either direction.[Abstract] [Full Text] [Related] [New Search]