Loss of MECP2 Leads to Activation of P53 and Neuronal Senescence.

A cell culture model of Rett Syndrome was accomplished as a disease-in-a-dish. Skin cells from Rett Syndrome patients were reprogrammed to stem cells, and then further induced to become nerve cells. A set of cells were mutated in candidate genes for causing Rett Syndrome in order to confirm that this culture system could be used to provide further insight into this disease.