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Reversion of FMR1 Methylation and Silencing by Editing the Triplet Repeats in Fragile X iPSC-Derived Neurons - ScienceDirect
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What Causes Fragile X Syndrome: Understanding the Genetic and Molecular Basis of the Condition • FRAXA Research Foundation - Finding a Cure for Fragile X Syndrome
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Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles. | Semantic Scholar
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Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome - The Lancet Neurology
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Most individuals in the general population have between 5 and 54 CGG... | Download Scientific Diagram
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Genes | Free Full-Text | Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome
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