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.
Citazione stile Chigago Style (17a edizione)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.
Citatione MLA (9a 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.
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