Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype. Submitted by iguillen on Tue, 06/25/2019 - 12:16 Lucariello M, Vidal E, Vidal S, et al. Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype. Hum Genet. 2016;135(12):1343-1354. doi:10.1007/s00439-016-1721-3.
Dysfunctional mitochondrial fission impairs cell reprogramming. Submitted by iguillen on Mon, 06/10/2019 - 12:04 Prieto J, León M, Ponsoda X, et al. Dysfunctional mitochondrial fission impairs cell reprogramming. Cell Cycle. 2016;15(23):3240-3250. doi:10.1080/15384101.2016.1241930.