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血管性血友病因子基因第40内含子中ATCT可变数目串联重复序列位点VWF.VNTR I的两个新等位基因。

Two novel alleles of the ATCT variable number tandem repeat locus VWF.VNTR I in intron 40 of the von Willebrand factor gene.

作者信息

Haddad A P, Sparrow R L

机构信息

Development Unit, Red Cross Blood Bank Victoria, Southbank, Australia.

出版信息

Br J Haematol. 1997 Feb;96(2):298-300. doi: 10.1046/j.1365-2141.1997.d01-2026.x.

Abstract

Two new alleles, allele 9 and allele 15, of the ATCT variable number tandem repeat locus, VWF.VNTR I, of intron 40 of the von Willebrand factor (VWF) gene are described. Both alleles occurred in low frequencies, being detected in only two and one of 285 random Australian Caucasians respectively. In all, 10 alleles were observed representing between six and 15 repeats of the ATCT motif. The allele frequency distribution in this Australian population was similar to other VWF.VNTR I population studies. The additional alleles described here for the VWF.VNTR I further enhance the usefulness of this VNTR locus in human identification work.

摘要

描述了血管性血友病因子(VWF)基因第40内含子的ATCT可变数目串联重复序列位点VWF.VNTR I的两个新等位基因,即等位基因9和等位基因15。这两个等位基因出现频率较低,分别在285名澳大利亚随机白种人中仅检测到2例和1例。总共观察到10个等位基因,代表ATCT基序的6至15次重复。该澳大利亚人群中等位基因频率分布与其他VWF.VNTR I人群研究相似。这里描述的VWF.VNTR I的额外等位基因进一步提高了该VNTR位点在人类身份鉴定工作中的实用性。

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