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中国汉族特发性震颤患者融合肉瘤基因的遗传分析。

Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor.

机构信息

Center for Experimental Medicine, the Third Xiangya Hospital, Central South University, Changsha, China.

出版信息

Neurobiol Aging. 2013 Aug;34(8):2078.e3-4. doi: 10.1016/j.neurobiolaging.2013.03.001. Epub 2013 Apr 9.

Abstract

We conducted genetic analysis of the fused in sarcoma gene (FUS) in Chinese Han patients with essential tremor (ET) in a case-control association study. One hundred eighty unrelated patients with ET were screened for mutations in the coding region and exon-intron boundaries of FUS. Reverse transcriptase polymerase chain reaction analysis was performed to evaluate if the c.1176G>A variant results in change of splice site. Two hundred seventy-three normal control subjects were also analyzed when DNA variants were identified in ET cohort. A novel missense mutation, c.1176G>A (p.M392I), in FUS was identified in a 62-year-old patient. Four known variants (c.52C>A, p.P18T; c.147C>A, p.G49G; c.291T>C, p.Y97Y; c.684C>T, p.G228G) were observed in the case-control study without statistically significant differences in genotype and allele distributions. Mutation(s) in FUS might be associated with a small subset of ET cases in the Chinese population.

摘要

我们在一项病例对照关联研究中对融合肉瘤基因(FUS)进行了遗传分析,研究对象为汉族原发性震颤(ET)患者。我们筛选了 180 名无血缘关系的 ET 患者,以检测 FUS 编码区和外显子-内含子边界的突变。采用逆转录聚合酶链反应分析评估 c.1176G>A 变异是否导致剪接位点改变。当在 ET 队列中发现 DNA 变异时,我们还分析了 273 名正常对照。在一名 62 岁患者中发现了 FUS 的一种新错义突变 c.1176G>A(p.M392I)。在病例对照研究中观察到了四个已知的变异(c.52C>A,p.P18T;c.147C>A,p.G49G;c.291T>C,p.Y97Y;c.684C>T,p.G228G),但基因型和等位基因分布无统计学差异。FUS 的突变可能与中国人群中的一小部分 ET 病例有关。

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