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Genome-wide association study identified genetic variants associated with severity of COPD in Korean participants

机译:基因组关联研究确定了与韩国参与者的COPD严重程度相关的遗传变异

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Chronic Obstructive Pulmonary Diseases (COPD) is a complex disease with considerable variability affecting about 65 million individuals [1]. We therefore performed a genome-wide association study (GWAS) of COPD severity. Thirty-four genetic variants were identified (P <; 1.0×10-5), and were located in intron and upstream/downstream regions. In conclusion, these genetic markers could provide insight into the understanding the pathological process of COPD.
机译:慢性阻塞性肺病(COPD)是一种复杂的疾病,影响了约6500万个体的可变性[1]。因此,我们进行了一种基因组 - 宽协会研究(GWA)的COPD严重程度。鉴定了三十四种遗传变异(P <; 1.0×10 -5 ),并位于内含子和上游/下游区域。总之,这些遗传标志物可以洞察理解COPD的病理过程。

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