APA Alıntı

Xu, X., Yang, X., Wu, Q., Liu, A., Yang, X., Ye, A. Y., . . . Zhang, Y. (2015). Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de novo” SCN1A Mutations in Children with Dravet Syndrome. Hum Mutat.

Chicago Stili Alıntı

Xu, Xiaojing, et al. "Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de Novo” SCN1A Mutations in Children With Dravet Syndrome." Hum Mutat 2015.

MLA Alıntı

Xu, Xiaojing, et al. "Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de Novo” SCN1A Mutations in Children With Dravet Syndrome." Hum Mutat 2015.