首页> 外文期刊>Neurology Research International >High-Resolution Melting (HRM) Analysis of the Cu/Zn Superoxide Dismutase (SOD1) Gene in Japanese Sporadic Amyotrophic Lateral Sclerosis (SALS) Patients
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High-Resolution Melting (HRM) Analysis of the Cu/Zn Superoxide Dismutase (SOD1) Gene in Japanese Sporadic Amyotrophic Lateral Sclerosis (SALS) Patients

机译:日本散发性肌萎缩性侧索硬化症(SALS)患者中Cu / Zn超氧化物歧化酶(SOD1)基因的高分辨率熔解(HRM)分析

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Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder, and the majority of ALS are sporadic (SALS). Recently, several causative genes for familial ALS (FALS) were identified, but the cause of the SALS is still unknown. This time, we aimed to identify the genetic background of SALS. First, we applied the new sensitive screening methods: high-resolution melting (HRM) analysis. HRM analysis detected 18 out of 19 known SOD1 gene mutations (94.7%sensitivity). Next, we screenedSOD1, three novel mutations (C6Y, Q22H, and S134T) were identified in our own 184 SALS cases (1.63%prevalence), and four mutations in another 255 SALS cases (1.56%prevalence) registered from all over Japan. The patients withSOD1mutations suggested a relatively young onset and limb involvement at onset. The HRM analysis is a sensitive and easy screening method; we will use this method for screening other ALS causative genes and revealing the genetic background of SALS.
机译:肌萎缩性侧索硬化症(ALS)是一种进行性神经退行性疾病,大多数ALS是散发性(SALS)。最近,已鉴定出几种家族性ALS(FALS)的致病基因,但尚不清楚SALS的病因。这次,我们旨在鉴定SALS的遗传背景。首先,我们应用了新的敏感筛选方法:高分辨率熔解(HRM)分析。 HRM分析检测出19种已知SOD1基因突变中的18种(敏感性为94.7%)。接下来,我们筛选了SOD1,在我们自己的184例SALS病例中发现了3个新突变(C6Y,Q22H和S134T)(患病率为1.63%),在日本全国范围内登记的另外255例SALS病例中发现了4个突变(患病率为1.56%)。具有SOD1突变的患者建议发病相对较年轻,发病时肢体受累。 HRM分析是一种敏感且容易筛选的方法;我们将使用此方法筛选其他ALS致病基因并揭示SALS的遗传背景。

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