Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype
Mario Lucariello, Enrique Vidal, Silvia M. Vidal, Mauricio A. Sáez, Laura M. Roa, Dori Huertas, Mercè Pineda, Esther Dalfó, Joaquı́n Dopazo, Paola Jurado, Judith Armstrong, Manel Esteller (2016). Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype. , 135(12), DOI: https://doi.org/10.1007/s00439-016-1721-3.
