Cita APA (7th ed.)

Zhong, D., Huang, X., Feng, T., Zeng, J., Gu, S., Ning, F., . . . Ma, G. (2024). Congenital disorder of glycosylation type Ia in a Chinese family: Function analysis of a novel PMM2 complex heterozygosis mutation. Elsevier.

Cita Chicago (17th ed.)

Zhong, Dan, et al. Congenital Disorder of Glycosylation Type Ia in a Chinese Family: Function Analysis of a Novel PMM2 Complex Heterozygosis Mutation. Elsevier, 2024.

Cita MLA (9th ed.)

Zhong, Dan, et al. Congenital Disorder of Glycosylation Type Ia in a Chinese Family: Function Analysis of a Novel PMM2 Complex Heterozygosis Mutation. Elsevier, 2024.