Cita APA (7a ed.)

Li, Y., Zhao, X., Wang, S., Xu, K., Zhao, X., Huang, S., & Zhu, S. (2021). A Novel Loss-of-Function Mutation in the NPRL3 Gene Identified in Chinese Familial Focal Epilepsy with Variable Foci. Frontiers Media S.A.

Cita Chicago Style (17a ed.)

Li, Youzhi, Xu Zhao, Shanshan Wang, Ke Xu, Xin Zhao, Shanshan Huang, y Suiqiang Zhu. A Novel Loss-of-Function Mutation in the NPRL3 Gene Identified in Chinese Familial Focal Epilepsy with Variable Foci. Frontiers Media S.A, 2021.

Cita MLA (8a ed.)

Li, Youzhi, et al. A Novel Loss-of-Function Mutation in the NPRL3 Gene Identified in Chinese Familial Focal Epilepsy with Variable Foci. Frontiers Media S.A, 2021.