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HLA I类基因座:遗传性血色素沉着症中限制性片段长度多态性分析

The HLA class I locus: analysis of RFLPs in hereditary hemochromatosis.

作者信息

Hansen J L, Kushner J P

机构信息

University of Utah College of Medicine, Salt Lake City.

出版信息

Cytogenet Cell Genet. 1989;50(4):216-9. doi: 10.1159/000132763.

Abstract

The gene for hereditary hemochromatosis is linked to the HLA locus on chromosome 6. Four cloned DNA probes originating from the HLA class I region were used to detect seven restriction fragment length polymorphisms (RFLPs). Allele frequencies and segregation of each RFLP was determined. Analysis of RFLPs in 38 unrelated homozygotes with hemochromatosis revealed differences in allele frequencies between the control and the hemochromatotic groups but these differences did not reach statistical significance. Some differences persisted, however, even when only controls with the A3 antigen were compared with A3 hemochromatotics. Since both control and hemochromatotic groups were small, further studies will be necessary to ascertain whether these RFLPs could serve to locate the gene responsible for hereditary hemochromatosis.

摘要

遗传性血色素沉着症基因与6号染色体上的HLA位点相连。使用源自HLA I类区域的四个克隆DNA探针来检测七种限制性片段长度多态性(RFLP)。确定了每个RFLP的等位基因频率和分离情况。对38名无亲缘关系的血色素沉着症纯合子的RFLP分析显示,对照组和血色素沉着症组之间的等位基因频率存在差异,但这些差异未达到统计学意义。然而,即使仅将具有A3抗原的对照组与A3血色素沉着症患者进行比较,一些差异仍然存在。由于对照组和血色素沉着症组都较小,因此需要进一步研究以确定这些RFLP是否可用于定位导致遗传性血色素沉着症的基因。

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