Relationship between SNP rs1764391 and Susceptibility, Risk Factors, Gene-environment Interactions of Acute Myocardial Infarction in Guangxi Han Chinese Population.

CONCLUSIONS: The TT genotype of Cx37 SNP rs1764391 was identified as a predisposing factor for AMI, especially in women. This genetic variant may prove to be an important tool for AMI risk stratification, and thus might be a useful target for therapeutic intervention to further improve prognosis in high-risk patients. PMID: 31580250 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/31580250?dopt=Abstract

Source: Current Pharmaceutical Biotechnology - October 2, 2019 Category: Biotechnology Authors: Li J, Qin R, Wang W, Huang Z, Huang DL, Li T, Wang F, Zeng XT, Sun ZY, Liu XF, Huang F, Guo T Tags: Curr Pharm Biotechnol Source Type: research