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位于14号染色体长臂上、靠近α1-抗糜蛋白酶基因的家族性早发性阿尔茨海默病的一个基因座。

A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin gene.

作者信息

Mullan M, Houlden H, Windelspecht M, Fidani L, Lombardi C, Diaz P, Rossor M, Crook R, Hardy J, Duff K

机构信息

Alzheimer's Disease Research Laboratories, University of South Florida, Tampa 33613.

出版信息

Nat Genet. 1992 Dec;2(4):340-2. doi: 10.1038/ng1292-340.

Abstract

Although mutations in the beta-amyloid precursor protein gene (APP) on chromosome 21 cause some cases of early-onset Alzheimer's disease (AD), most cases evidently do not have mutations in APP. We analysed ten early-onset families for linkage to APP and markers elsewhere in the genome. One family (F172) was consistent with linkage to chromosome 21 and was subsequently found to have an APP Val to Ile mutation. Of the others, all but one were consistent with linkage to markers in the middle long arm of chromosome 14. However, no family showed independent evidence of linkage with two point analysis and only one showed independent evidence of linkage on multipoint analysis. Therefore, we cannot rule out heterogeneity at these loci although tests for heterogeneity were not significant.

摘要

尽管21号染色体上的β-淀粉样前体蛋白基因(APP)突变会导致某些早发性阿尔茨海默病(AD)病例,但大多数病例显然没有APP突变。我们分析了10个早发性家系与APP及基因组其他位置标记的连锁情况。一个家系(F172)与21号染色体连锁一致,随后发现有APP缬氨酸到异亮氨酸的突变。在其他家系中,除一个外,所有家系都与14号染色体长臂中部的标记连锁一致。然而,没有一个家系在两点分析中显示出独立的连锁证据,只有一个家系在多点分析中显示出独立的连锁证据。因此,尽管异质性检验不显著,但我们不能排除这些位点存在异质性。

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