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Genetic studies of human apolipoproteins. III. Polymorphism of apolipoprotein C-II.

作者信息

Sepehrnia B, Kamboh M I, Ferrell R E

机构信息

Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pa.

出版信息

Hum Hered. 1988;38(3):136-43. doi: 10.1159/000153774.

Abstract

Using a simple and rapid one-dimensional isoelectric focusing technique followed by immunoblotting, we have detected genetic polymorphism of human apolipoprotein C-II (APO C-II) in normal unfractionated plasma samples of individuals of black ancestry. Two common autosomal codominantly expressed alleles, designated APO C-II1 and APO C-II2, at the APO C-II structural locus have been observed with frequencies of 0.975 and 0.025 in US blacks and 0.943 and 0.049 in Nigerian blacks. In addition, the gene product of a rare allele designated APO C-II3 was observed in a single Nigerian black. Apart from a single example of an APO C-II 2-1 phenotype in plasma samples from 187 whites, which was electrophoretically identical to the 2-1 phenotype observed in blacks, it appears that APO C-II2 is a unique black marker of potential importance in anthropogenetic and atherosclerosis studies.

摘要

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