Cite
Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency.
MLA
Hall, Patricia L., et al. “Urine Oligosaccharide Screening by MALDI-TOF for the Identification of NGLY1 Deficiency.” Molecular Genetics & Metabolism, vol. 124, no. 1, May 2018, pp. 82–86. EBSCOhost, https://doi.org/10.1016/j.ymgme.2018.03.002.
APA
Hall, P. L., Lam, C., Alexander, J. J., Asif, G., Berry, G. T., Ferreira, C., Freeze, H. H., Gahl, W. A., Nickander, K. K., Sharer, J. D., Watson, C. M., Wolfe, L., & Raymond, K. M. (2018). Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency. Molecular Genetics & Metabolism, 124(1), 82–86. https://doi.org/10.1016/j.ymgme.2018.03.002
Chicago
Hall, Patricia L., Christina Lam, John J. Alexander, Ghazia Asif, Gerard T. Berry, Carlos Ferreira, Hudson H. Freeze, et al. 2018. “Urine Oligosaccharide Screening by MALDI-TOF for the Identification of NGLY1 Deficiency.” Molecular Genetics & Metabolism 124 (1): 82–86. doi:10.1016/j.ymgme.2018.03.002.