APA citiranje

Byun, C. K., Lee, J. S., Lim, B. C., Kim, K. J., Hwang, Y. S., & Chae, J. (2015). FOXG1 Mutation is a Low-Incidence Genetic Cause in Atypical Rett Syndrome. Child Neurol Open.

Citação norma Chicago

Byun, Christine K., Jin Sook Lee, Byung Chan Lim, Ki Joong Kim, Yong Seung Hwang, and Jong-Hee Chae. "FOXG1 Mutation Is a Low-Incidence Genetic Cause in Atypical Rett Syndrome." Child Neurol Open 2015.

MLA citiranje

Byun, Christine K., et al. "FOXG1 Mutation Is a Low-Incidence Genetic Cause in Atypical Rett Syndrome." Child Neurol Open 2015.