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.
Chicago Style (17th ed.) CitationZhou, 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.
MLA (8th ed.) CitationZhou, 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.
Warning: These citations may not always be 100% accurate.