Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia

• المؤلفون الرئيسيون: Han Y., Dorajoo R., Chang X., Wang L., Khor C.-C., Sim X., Cheng C.-Y., Shi Y., Tham Y.C., Zhao W., Chee M.L., Sabanayagam C., Chae M.L., Tan N., Wong T.Y., Tai E.-S., Liu J., Goh D.Y.T., Yuan J.-M., Koh W.-P., Van Dam R.M., Low A.F., Chan M.Y.-Y., Friedlander Y., Heng C.-K.
• مؤلفون آخرون: MEDICINE
• التنسيق: مقال
• منشور في: 2020
• الموضوعات: APOA5 protein, human; apolipoprotein A5; biological marker; adult; aged; case control study; coronary artery disease; ethnic group; ethnology; female; follow up; genetic predisposition; genetics; genome-wide association study; genotype; human; male; metabolism; middle aged; missense mutation; procedures; prognosis; prospective study; single nucleotide polymorphism; Southeast Asia; very elderly; Adult; Aged; Aged, 80 and over; Apolipoprotein A-V; Asia, Southeastern; Biomarkers; Case-Control Studies; Coronary Artery Disease; Ethnic Groups; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Humans; Male; Middle Aged; Mutation, Missense; Polymorphism, Single Nucleotide; Prognosis; Prospective Studies
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/175085

10.1038/s41598-017-18214-z