Association of MTHFD1 G1958A (rs2236225) gene polymorphism with the risk of congenital heart disease: a systematic review and meta-analysis.

MLA

Yi, Kang, et al. “Association of MTHFD1 G1958A (Rs2236225) Gene Polymorphism with the Risk of Congenital Heart Disease: A Systematic Review and Meta-Analysis.” BMC Medical Genomics, vol. 18, no. 1, Jan. 2025, p. 20. EBSCOhost, https://doi.org/10.1186/s12920-024-02052-w.

APA

Yi, K., He, S.-E., Guo, T., Wang, Z.-Q., Zhang, X., Xu, J.-G., Zhang, H.-Y., Liu, W.-G., & You, T. (2025). Association of MTHFD1 G1958A (rs2236225) gene polymorphism with the risk of congenital heart disease: a systematic review and meta-analysis. BMC Medical Genomics, 18(1), 20. https://doi.org/10.1186/s12920-024-02052-w

Chicago

Yi, Kang, Shao-E He, Tao Guo, Zi-Qiang Wang, Xin Zhang, Jian-Guo Xu, Hao-Yue Zhang, Wei-Guo Liu, and Tao You. 2025. “Association of MTHFD1 G1958A (Rs2236225) Gene Polymorphism with the Risk of Congenital Heart Disease: A Systematic Review and Meta-Analysis.” BMC Medical Genomics 18 (1): 20. doi:10.1186/s12920-024-02052-w.