Skip to main content

ME Kleinman

First name:
ME
Last name:
Kleinman
Gordon, L. B., Campbell, S. E., Massaro, J. M., RB, D. 'A., Kleinman, M. E., Kieran, M. W., & Moses, M. A. (2018). Survey of plasma proteins in children with progeria pre-therapy and on-therapy with lonafarnib. Pediatric Research. https://doi.org/10.1038/pr.2018.9 (Original work published 2018)
Zhong, Y., Mohan, K., Liu, J., Al-Attar, A., Lin, P., Flight, R. M., et al. (2020). Loss of CLN3, the gene mutated in juvenile neuronal ceroid lipofuscinosis, leads to metabolic impairment and autophagy induction in retinal pigment epithelium. Biochimica Et Biophysica Acta. Molecular Basis Of Disease, 1866(10), 165883. https://doi.org/10.1016/j.bbadis.2020.165883 (Original work published 2020)