APA (7th ed.) Citation

Haixia Ge, Qingbin Wu, Huigang Lu, Yong Huang, Tingting Zhou, Danlin Tan, & ZhongqinJin. (2020). Two novel compound heterozygous mutations in NGLY1as a cause of congenital disorder of deglycosylation: A case presentation. BMC.

Chicago Style (17th ed.) Citation

Haixia Ge, Qingbin Wu, Huigang Lu, Yong Huang, Tingting Zhou, Danlin Tan, and ZhongqinJin. Two Novel Compound Heterozygous Mutations in NGLY1as a Cause of Congenital Disorder of Deglycosylation: A Case Presentation. BMC, 2020.

MLA (9th ed.) Citation

Haixia Ge, et al. Two Novel Compound Heterozygous Mutations in NGLY1as a Cause of Congenital Disorder of Deglycosylation: A Case Presentation. BMC, 2020.