Cite
A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype.
MLA
Iqbal, Zafar, et al. “A Compound Heterozygous Mutation in DPAGT1 Results in a Congenital Disorder of Glycosylation with a Relatively Mild Phenotype.” European Journal of Human Genetics, vol. 21, no. 8, Aug. 2013, pp. 844–49. EBSCOhost, https://doi.org/10.1038/ejhg.2012.257.
APA
Iqbal, Z., Shahzad, M., Vissers, L. E. L. M., van Scherpenzeel, M., Gilissen, C., Razzaq, A., Zahoor, M. Y., Khan, S. N., Kleefstra, T., Veltman, J. A., de Brouwer, A. P. M., Lefeber, D. J., van Bokhoven, H., & Riazuddin, S. (2013). A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype. European Journal of Human Genetics, 21(8), 844–849. https://doi.org/10.1038/ejhg.2012.257
Chicago
Iqbal, Zafar, Mohsin Shahzad, Lisenka E L M Vissers, Monique van Scherpenzeel, Christian Gilissen, Attia Razzaq, Muhammad Yasir Zahoor, et al. 2013. “A Compound Heterozygous Mutation in DPAGT1 Results in a Congenital Disorder of Glycosylation with a Relatively Mild Phenotype.” European Journal of Human Genetics 21 (8): 844–49. doi:10.1038/ejhg.2012.257.