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.
Chicago Style (17th ed.) CitationLi, Youzhi, Xu Zhao, Shanshan Wang, Ke Xu, Xin Zhao, Shanshan Huang, and 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.
MLA (8th ed.) CitationLi, 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.
Warning: These citations may not always be 100% accurate.