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Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype

Authors:	Mario Lucariello Enrique Vidal Silvia Vidal Mauricio Saez Laura Roa Dori Huertas Mercè Pineda Esther Dalfó Joaquin Dopazo Paola Jurado Judith Armstrong Manel Esteller

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