TARDBP公司
C9orf72
肌萎缩侧索硬化
SOD1
荟萃分析
医学
遗传学
生物
突变
遗传流行病学
突变频率
疾病
基因
病理
三核苷酸重复扩增
等位基因
作者
Zhang‐Yu Zou,Zhi-Rui Zhou,Chun-Hui Che,Chang-Yun Liu,Rao-Li He,Hua-Pin Huang
标识
DOI:10.1136/jnnp-2016-315018
摘要
BACKGROUND: are the most common mutated genes in amyotrophic lateral sclerosis (ALS). Here, we performed a meta-analysis to determine the mutation frequencies of these major ALS-related genes in patients with ALS. METHODS: mutations in ALS. The mutation frequency and effect size of each study were combined. Possible sources of heterogeneity across studies were determined by meta-regression, sensitivity analysis and subgroup analysis. RESULTS: (FALS 1.5%, SALS 0.2%) mutations. CONCLUSIONS: These findings demonstrated that the genetic architecture of ALS in Asian populations is distinct from that in European populations, which need to be given appropriate consideration when performing genetic testing of patients with ALS.
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