Trích dẫn APA

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 Chicago

Lu, 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 MLA

Lu, 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.

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