GENETIC-POLYMORPHISM OF HUMAN-SERUM TRANSFERRIN IN THE SWISS POPULATION - EVIDENCE FOR 3 NEW TRANSFERRIN-VARIANTS

被引:6
作者
SCHERZ, R
REBER, B
PFLUGSHAUPT, R
BUTLER, R
机构
[1] Blood Transfusion Service, Src, Central Laboratory, Bern
关键词
D O I
10.1002/elps.1150061112
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Genetic polymorphism of transferrin (Tf) was studied in 473 healthy Swiss blood donors and 236 nonrelated individuals engaged in cases of disputed paternity. Gene frequencies were: TfC1 = 0.7727, TfC2 = 0.1634, TfC3 = 0.0573. Several rare alleles were observed, the frequency of the total of which was 0.0066. Three obviously new Tf alleles were detected. The phenotype distribution was in agreement with the Hardy Weinberg equilibrium. Among 113 mother/child pairs no phenotypes contradictory to the mendelian law were observed. The transferrin system represents a useful parameter in routine paternity testing. Its average chance of exclusion (without rare alleles) is 18.19%. Copyright © 1985 VCH Verlagsgesellschaft mbH
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收藏
页码:569 / 571
页数:3
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