Zhao, N., Yang, Y., Li, P., Xiong, Q., Xiao, H., & Wu, C. (2021). Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott–Rallison Syndrome in a Chinese Family. Front Pediatr.
Citación estilo ChicagoZhao, Na, Yanling Yang, Ping Li, Qiuhong Xiong, Han Xiao, and Changxin Wu. "Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott–Rallison Syndrome in a Chinese Family." Front Pediatr 2021.
Cita MLAZhao, Na, et al. "Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott–Rallison Syndrome in a Chinese Family." Front Pediatr 2021.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.