APA (7th ed.) Citation

Meng, L., Fang, Z., Jiang, L., Zheng, Y., Hong, S., Deng, Y., & Xie, L. Heterozygous pathogenic STT3A variation leads to dominant congenital glycosylation disorders and functional validation in zebrafish. BMC.

Chicago Style (17th ed.) Citation

Meng, Linxue, Zhixu Fang, Li Jiang, Yinglan Zheng, Siqi Hong, Yu Deng, and Lingling Xie. Heterozygous Pathogenic STT3A Variation Leads to Dominant Congenital Glycosylation Disorders and Functional Validation in Zebrafish. BMC.

MLA (9th ed.) Citation

Meng, Linxue, et al. Heterozygous Pathogenic STT3A Variation Leads to Dominant Congenital Glycosylation Disorders and Functional Validation in Zebrafish. BMC.