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对爱尔兰乳糜泻患者及对照进行免疫球蛋白重链同种异型分型无助于定位“第二个”乳糜泻基因。

Gm typing of Irish coeliac patients and controls does not help locate the "second" coeliac gene.

作者信息

Hannigan M, Bourke M, Stevens F M, McCarthy C F

机构信息

University Department of Medicine, University College Hospital, Galway, Ireland.

出版信息

Ir J Med Sci. 1991 Feb;160(2):57-8. doi: 10.1007/BF02947649.

Abstract

A two gene model has been proposed to explain the inheritance of coeliac disease (CD). One gene is on chromosome 6 in the MHC complex (HLA associated). It has been suggested the second gene is located on chromosome 14, in or near the region encoding for immunoglobulin heavy chain allotypes (Gm types). In a study of 102 unrelated Irish coeliacs and a group of ethnic controls, we have failed to show an association of CD with any particular Gm type or types. There is no evidence to confirm that a gene on chromosome 14 is implicated in the inheritance of CD.

摘要

有人提出了一种双基因模型来解释乳糜泻(CD)的遗传方式。一个基因位于MHC复合体的6号染色体上(与HLA相关)。有人认为第二个基因位于14号染色体上,在编码免疫球蛋白重链同种异型(Gm类型)的区域内或附近。在一项对102名无亲缘关系的爱尔兰乳糜泻患者和一组种族对照的研究中,我们未能发现CD与任何特定的Gm类型之间存在关联。没有证据证实14号染色体上的一个基因与CD的遗传有关。

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