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Schematic illustration of FMR1 gene. There are 17 alternatively spliced... | Download Scientific Diagram
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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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Antisense oligonucleotide rescue of CGG expansion–dependent FMR1 mis-splicing in fragile X syndrome restores FMRP | PNAS
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What Mechanisms Induce Methylation of FMR1 Gene Full Mutation? A Still Unanswered Question | SpringerLink
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Epigenetic Characterization of the FMR1 Gene and Aberrant Neurodevelopment in Human Induced Pluripotent Stem Cell Models of Fragile X Syndrome Video | LabTube
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Gene therapy using human FMRP isoforms driven by the human FMR1 promoter rescues fragile X syndrome mouse deficits: Molecular Therapy Methods & Clinical Development
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Frontiers | Long Noncoding RNA Can Be a Probable Mechanism and a Novel Target for Diagnosis and Therapy in Fragile X Syndrome
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FMR1 gene and FMRP protein structure. FMR1 contains a coding region... | Download Scientific Diagram
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FMR1 gene enhances the translation of large autism-related proteins - Jane Coffin Childs Memorial Fund
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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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Fragile X syndrome: An overview and update of the FMR1 gene - Mila - 2018 - Clinical Genetics - Wiley Online Library
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