Epigenetic Characterization of the FMR1 Gene and Aberrant Neurodevelopment in Human Induced Pluripot...
Epigenetic Characterization of the FMR1 Gene and Aberrant Neurodevelopment in Human Induced Pluripotent Stem Cell Models of Fragile X Syndrome
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United States: Public Library of Science
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English
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United States: Public Library of Science
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Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. In addition to cognitive deficits, FXS patients exhibit hyperactivity, attention deficits, social difficulties, anxiety, and other autistic-like behaviors. FXS is caused by an expanded CGG trinucleotide repeat in the 5' untranslated region of the Fragile X Menta...
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Epigenetic Characterization of the FMR1 Gene and Aberrant Neurodevelopment in Human Induced Pluripotent Stem Cell Models of Fragile X Syndrome
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TN_cdi_plos_journals_1309451682
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1309451682
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ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0026203
