Cita APA (7a ed.)

Zhou, B., Zhang, C., Zheng, L., Wang, Z., Chen, X., Feng, X., . . . Hui, L. (2021). Case Report: A Novel De Novo Missense Mutation of the GRIA2 Gene in a Chinese Case of Neurodevelopmental Disorder With Language Impairment. Frontiers Media S.A.

Cita Chicago Style (17a ed.)

Zhou, Bingbo, et al. Case Report: A Novel De Novo Missense Mutation of the GRIA2 Gene in a Chinese Case of Neurodevelopmental Disorder With Language Impairment. Frontiers Media S.A, 2021.

Cita MLA (8a ed.)

Zhou, Bingbo, et al. Case Report: A Novel De Novo Missense Mutation of the GRIA2 Gene in a Chinese Case of Neurodevelopmental Disorder With Language Impairment. Frontiers Media S.A, 2021.