Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity.

MLA

Adams, David R., et al. “Three Rare Diseases in One Sib Pair: RAI1, PCK1, GRIN2B Mutations Associated with Smith-Magenis Syndrome, Cytosolic PEPCK Deficiency and NMDA Receptor Glutamate Insensitivity.” Molecular Genetics and Metabolism, vol. 113, no. 3, Nov. 2014, pp. 161–70. EBSCOhost, https://doi.org/10.1016/j.ymgme.2014.04.001.

APA

Adams, D. R., Yuan, H., Holyoak, T., Arajs, K. H., Hakimi, P., Markello, T. C., Wolfe, L. A., Vilboux, T., Burton, B. K., Fajardo, K. F., Grahame, G., Holloman, C., Sincan, M., Smith, A. C. M., Wells, G. A., Huang, Y., Vega, H., Snyder, J. P., Golas, G. A., … Gahl, W. A. (2014). Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity. Molecular Genetics and Metabolism, 113(3), 161–170. https://doi.org/10.1016/j.ymgme.2014.04.001

Chicago

Adams, David R, Hongjie Yuan, Todd Holyoak, Katrina H Arajs, Parvin Hakimi, Thomas C Markello, Lynne A Wolfe, et al. 2014. “Three Rare Diseases in One Sib Pair: RAI1, PCK1, GRIN2B Mutations Associated with Smith-Magenis Syndrome, Cytosolic PEPCK Deficiency and NMDA Receptor Glutamate Insensitivity.” Molecular Genetics and Metabolism 113 (3): 161–70. doi:10.1016/j.ymgme.2014.04.001.