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早发型家族性阿尔茨海默病中淀粉样前体蛋白的突变分析

[Mutation analysis of amyloid precursor protein in early-onset familial Alzheimer's disease].

作者信息

Naruse S, Fujigasaki H, Miyatake T

机构信息

Department of Neurology, Tokyo Medical and Dental University.

出版信息

Nihon Rinsho. 1993 Sep;51(9):2445-51.

PMID:8411726
Abstract

Recently, three different mutations have been found at codon 717 of the amyloid precursor protein (APP) gene, changing the native valine to isoleucine, phenylalanine and glycine in some familial Alzheimer's disease (FAD) kindreds. More recently, some other mutations have also been reported at codons 670 and 671 (double mutation), and codon 692. As analysis of coding region except exon 16 and 17 has been insufficient in previous reports, we analyzed entire coding region of the APP gene of 6 Japanese early-onset FAD kindreds using automated sequencer. Three FAD families showed known 717 Val to Ile mutation, whereas no novel mutations were detected.

摘要

最近,在淀粉样前体蛋白(APP)基因的717密码子处发现了三种不同的突变,在一些家族性阿尔茨海默病(FAD)家系中,天然的缬氨酸被异亮氨酸、苯丙氨酸和甘氨酸取代。最近,在670和671密码子(双重突变)以及692密码子处也报道了一些其他突变。由于之前的报告对除第16和17外显子的编码区分析不足,我们使用自动测序仪分析了6个日本早发性FAD家系的APP基因的整个编码区。三个FAD家族显示出已知的717缬氨酸到异亮氨酸的突变,而未检测到新的突变。

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