Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency.

MLA

Zhen, Xin, et al. “Molecular and Clinical Characterization of a Founder Mutation Causing G6PC3 Deficiency.” MedRxiv : The Preprint Server for Health Sciences, May 2024. EBSCOhost, https://doi.org/10.1101/2024.05.13.24307299.

APA

Zhen, X., Betti, M. J., Kars, M. E., Patterson, A., Medina-Torres, E. A., Scheffler Mendoza, S. C., Herrera Sánchez, D. A., Lopez-Herrera, G., Svyryd, Y., Mutchinick, O. M., Gamazon, E., Rathmell, J. C., Itan, Y., Markle, J., O’Farrill Romanillos, P., Lugo-Reyes, S. O., & Martinez-Barricarte, R. (2024). Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency. MedRxiv : The Preprint Server for Health Sciences. https://doi.org/10.1101/2024.05.13.24307299

Chicago

Zhen, Xin, Michael J Betti, Meltem Ece Kars, Andrew Patterson, Edgar Alejandro Medina-Torres, Selma Cecilia Scheffler Mendoza, Diana Andrea Herrera Sánchez, et al. 2024. “Molecular and Clinical Characterization of a Founder Mutation Causing G6PC3 Deficiency.” MedRxiv : The Preprint Server for Health Sciences, May. doi:10.1101/2024.05.13.24307299.