Suppr超能文献

常染色体隐性少年型帕金森病(PARK2)家族中D6S305的微缺失。

A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2).

作者信息

Matsumine H, Yamamura Y, Hattori N, Kobayashi T, Kitada T, Yoritaka A, Mizuno Y

机构信息

Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.

出版信息

Genomics. 1998 Apr 1;49(1):143-6. doi: 10.1006/geno.1997.5196.

Abstract

A gene for autosomal recessive juvenile parkinsonism (ARJP; HGMW-approved symbol PARK2; MIM 600116) has recently been mapped to a 17-cM interval on chromosome 6q25.2-q27. We here report an inbred family with ARJP showing a perfect cosegregation with null allele for D6S305, which is a marker within the ARJP locus. We assigned the deletion within an interval between D6S1937 and AFMa155td9, which are 0 cM apart from each other and located on a single YAC clone. Two possibilities should be evaluated: (1) the deletion is polymorphic and linked to ARJP and (2) the deletion is pathogenic and contains both D6S305 and the ARJP gene (or a part of it). An exon search in a deleted segment or in the relatively small-sized genomic clones harboring D6S305 may enormously facilitate the cloning procedure of the ARJP gene.

摘要

一种常染色体隐性少年帕金森病(ARJP;HGMW批准符号为PARK2;MIM 600116)的基因最近被定位到6号染色体6q25.2 - q27上一个17厘摩的区间。我们在此报告一个患有ARJP的近亲家族,该家族显示与D6S305的无效等位基因完全共分离,D6S305是ARJP基因座内的一个标记。我们将缺失定位在D6S1937和AFMa155td9之间的一个区间内,这两个标记彼此相距0厘摩,且位于单个酵母人工染色体(YAC)克隆上。应评估两种可能性:(1)该缺失是多态性的且与ARJP连锁;(2)该缺失是致病性的,并且包含D6S305和ARJP基因(或其一部分)。在缺失片段或携带D6S305的相对小尺寸基因组克隆中进行外显子搜索可能极大地促进ARJP基因的克隆过程。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验