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法国两个群体诺曼人和巴斯克人中人类C3和备解素因子B的同种异型变体。

Allotypic variants of human C3 and properdin factor B in two French populations Normans and Basques.

作者信息

Davrinche C, Rivat C, Rivat-Peran L

出版信息

Rev Fr Transfus Immunohematol. 1981 Jun;24(3):309-17. doi: 10.1016/s0338-4535(81)80210-3.

Abstract

Human Properdin factor B and C3 polymorphisms are of a real usefulness as genetic markers for population studies. In addition, they are more and more used for the determination of paternity cases. The present communication will be about Bf and C3 allele frequencies in two locally populations of France, Normandy and Western Pyrenees (Basques), The corresponding allele frequencies are as follows, for Normans : Bf(S) = 0.7422, Bf(F) = 0.2285, Bf(F1) = 0.0205, Bf(SO.7) = 0.0088; CsS = 0.788, C3F = 0.204, C3Srare = 0.004, C3Frare =0.004; and for Basques : BfS = 0.5625, BfF = 0.305, BfF1 = 0.1235, BfSO.7 = 0.0075; C3S = 0.7075 and C3F - 0.2925. French Basques are characterized by unusual allele frequencies in European Caucasoid populations for Bf as for C3 genes. A very high incidence of BfF1 allele is reported (BfF1 = 0.125), as previously observed [7, 17].

摘要

人类备解素因子B和C3多态性作为群体研究的遗传标记具有实际用途。此外,它们越来越多地用于亲子鉴定案件的判定。本报告将涉及法国诺曼底和西比利牛斯地区(巴斯克人)两个当地群体中Bf和C3等位基因频率。诺曼人的相应等位基因频率如下:Bf(S)=0.7422,Bf(F)=0.2285,Bf(F1)=0.0205,Bf(SO.7)=0.0088;C3S=0.788,C3F=0.204,C3Srare=0.004,C3Frare=0.004;巴斯克人的相应等位基因频率如下:BfS=0.5625,BfF=0.305,BfF1=0.1235,BfSO.7=0.0075;C3S=0.7075,C3F=0.2925。法国巴斯克人在欧洲白种人群体中,其Bf和C3基因的等位基因频率具有独特性。据报道,BfF1等位基因的发生率非常高(BfF1=0.125),如先前观察到的[7,17]。

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