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Adams, D.R., Yuan, H., Holyoak, T., Arajs, K.H., Hakimi, P., Markello, T.C., 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, 161-170.
https://doi.org/10.1016/j.ymgme.2014.04.001

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