Human iPSC-derived cerebral organoids model features of Leigh Syndrome and reveal abnormal corticogenesis
A. I. Romero-Morales, G. L. Robertson, A. Rastogi, M. L. Rasmussen, H. Temuri, R. P. Chakrabarty, G. S. McElroy, L. Hsu, P. M. Almonacid, B. A. Millis, N. S. Chandel, J.-P. Cartailler, V. Gama
This study uses iPSC-derived cerebral organoids to model Leigh Syndrome, identifying defects in brain development and mitochondrial morphology.
bioRxiv · Apr 21, 2020 · PreprintCell Biology