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分子生物学和基因组技术的发展为认识许多疾病真正的病因提供了新的方向及方法。目前对脑梗死发病机制的研究也已深入到基因水平。常用的方法为基于候选基因的关联研究,即将候选基因内的序列变异(常用SNP)做为遗传标志物,来分析其与疾病或某种表型之间的关系。由于动脉粥样硬化
The advances in molecular biology and genomics provide new directions and methods for understanding the true causes of many diseases. The current study of the pathogenesis of cerebral infarction has also been deep into the genetic level. Commonly used methods are based on the study of the association of candidate genes, that is, the sequence variation within the candidate gene (commonly used SNP) as a genetic marker to analyze its relationship with the disease or a certain phenotype. Due to atherosclerosis