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] Filters: Author is Vidal, Enrique and Keyword is Protein Serine-Threonine Kinases [Clear All Filters]
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.