Epigenetic Characterization of the FMR1 Gene and Aberrant Neurodevelopment in Human Induced Pluripotent Stem Cell Models of Fragile X Syndrome

Overview of attention for article published in PLOS ONE, October 2011

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Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. In addition to cognitive deficits, FXS…

http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0026203

http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0026203