Suppr超能文献

DJ1 分析在一大群意大利早发性帕金森病患者中。

DJ1 analysis in a large cohort of Italian early onset Parkinson Disease patients.

机构信息

Medical Genetics Laboratory, Foundation IRCCS "Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena", Milan, Italy.

出版信息

Neurosci Lett. 2013 Dec 17;557 Pt B(PB):165-70. doi: 10.1016/j.neulet.2013.10.048. Epub 2013 Oct 28.

Abstract

We analyzed the DJ1 gene in a large consecutive series (N=163) of Italian unrelated Early Onset Parkinson Disease (EOPD: onset ≤40 years of age) patients and 100 healthy controls (mean age 64 ± 7 years). No homozygous or compound heterozygous mutations with an obvious pathogenic effect were found. Several variants were identified, some of which were novels. All variants had similar frequency in patients and in controls. Our data suggest that DJ1 mutations are very rare in Italian EOPD. Other genes and risk factors for PD are still to be identified.

摘要

我们分析了一个由 163 例意大利散发性早发性帕金森病(EOPD:发病年龄≤40 岁)患者和 100 名健康对照组成的大型连续系列中的 DJ1 基因(平均年龄 64 ± 7 岁)。未发现具有明显致病作用的纯合子或复合杂合突变。发现了一些变异,其中一些是新的。所有变异在患者和对照组中的频率相似。我们的数据表明,DJ1 突变在意大利 EOPD 中非常罕见。PD 的其他基因和危险因素仍有待确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40bd/3878804/2a6e0970cd3e/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验