Lu, P., Ma, L., Sun, J., Gong, X., & Cai, C. (2021). A Chinese newborn with Zellweger syndrome and compound heterozygous mutations novel in the PEX1 gene: A case report and literature review. Transl Pediatr.
Trích dẫn kiểu ChicagoLu, Pei, Li Ma, Jingjing Sun, Xiaohui Gong, và Cheng Cai. "A Chinese Newborn With Zellweger Syndrome and Compound Heterozygous Mutations Novel in the PEX1 Gene: A Case Report and Literature Review." Transl Pediatr 2021.
Trích dẫn MLALu, Pei, et al. "A Chinese Newborn With Zellweger Syndrome and Compound Heterozygous Mutations Novel in the PEX1 Gene: A Case Report and Literature Review." Transl Pediatr 2021.
Cảnh báo: Các trích dẫn này có thể không phải lúc nào cũng chính xác 100%.