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Abstract Fragile X syndrome (FXS), the most commonly inherited form of mental retardation and autism, is caused by transcriptional silencing of the fragile X mental retardation 1 (FMR1) gene and consequent loss of the fragile X mental retardation protein. Despite growing evidence suggesting a role of specific receptors and biochemical pathways inFXS pathogenesis, an effective therapeutic method h
Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype Hiroki Kano*, Hiroki Kurahashi†, and Tatsushi Toda*,‡ *Division of Clinical Genetics, Department of Medical Genetics, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan; and †Division of Molecular Genetics, Institute for Comprehensive Medical Sci
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