A comprehensive in silico analysis, distribution and frequency of human Nkx2-5 mutations; A critical gene in congenital heart disease.

MLA

Kalayinia, Samira, et al. “A Comprehensive in Silico Analysis, Distribution and Frequency of Human Nkx2-5 Mutations; A Critical Gene in Congenital Heart Disease.” Journal of Cardiovascular and Thoracic Research, vol. 11, no. 4, 2019, pp. 287–99. EBSCOhost, https://doi.org/10.15171/jcvtr.2019.47.

APA

Kalayinia, S., Ghasemi, S., & Mahdieh, N. (2019). A comprehensive in silico analysis, distribution and frequency of human Nkx2-5 mutations; A critical gene in congenital heart disease. Journal of Cardiovascular and Thoracic Research, 11(4), 287–299. https://doi.org/10.15171/jcvtr.2019.47

Chicago

Kalayinia, Samira, Serwa Ghasemi, and Nejat Mahdieh. 2019. “A Comprehensive in Silico Analysis, Distribution and Frequency of Human Nkx2-5 Mutations; A Critical Gene in Congenital Heart Disease.” Journal of Cardiovascular and Thoracic Research 11 (4): 287–99. doi:10.15171/jcvtr.2019.47.