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美国马里兰大学的一个科研小组日前报告说,他们发现了一个与高血压有关的常见基因变异,这将帮助医学研究人员接照个人基因差异为高血压患者提供“个性化治疗”。研究小组在新一期美国《国家科学院学报》网络版上发表论文指出,这个基因名为STK39,位于2号染色体上。
A research team at the University of Maryland recently reported that they found a common genetic variant associated with hypertension that will help medical researchers adapt individual genetic differences to provide “personalized treatment” for hypertensive patients. The team published a paper in the new issue of the Proceedings of the National Academy of Sciences online that the gene is called STK39 and is located on chromosome 2.