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2017

Burnett, L. C., LeDuc, C. A., Sulsona, C. R., Paull, D., Rausch, R., Eddiry, S., et al. (2017). Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome. J Clin Invest, 127(1), 293–305.
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Lacovich, V., Espindola, S. L., Alloatti, M., Pozo Devoto, V., Cromberg, L. E., Carna, M. E., et al. (2017). Tau Isoforms Imbalance Impairs the Axonal Transport of the Amyloid Precursor Protein in Human Neurons. J Neurosci, 37(1), 58–69.
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Li, M., Zhao, H., Ananiev, G. E., Musser, M. T., Ness, K. H., Maglaque, D. L., et al. (2017). Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells. Stem Cells, 35(1), 158–169.
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Polex-Wolf, J., Yeo, G. S. H., & O'Rahilly, S. (2017). Impaired prohormone processing: a grand unified theory for features of Prader-Willi syndrome? J Clin Invest, 127(1), 98–99.
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Vershkov, D., & Benvenisty, N. (2017). Human pluripotent stem cells in modeling human disorders: the case of fragile X syndrome. Regen Med, 12(1), 53–68.
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