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Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset | Nature Neuroscience
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CAG-tract distributions of haplogroup variants. Only haplogroups with... | Download Scientific Diagram
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A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes - eBioMedicine
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Approaches to Sequence the HTT CAG Repeat Expansion and Quantify Repeat Length Variation - IOS Press
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Approaches to Sequence the HTT CAG Repeat Expansion and Quantify Repeat Length Variation - IOS Press
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Uninterrupted CAG repeat drives striatum-selective transcriptionopathy and nuclear pathogenesis in human Huntingtin BAC mice - ScienceDirect
Identification and Optimization of RNA-Splicing Modulators as Huntingtin Protein-Lowering Agents for the Treatment of Huntington's Disease | Journal of Medicinal Chemistry
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Development of a Self-Restricting CRISPR-Cas9 System to Reduce Off-Target Effects: Molecular Therapy Methods & Clinical Development
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Interrupting sequence variants and age of onset in Huntington's disease: clinical implications and emerging therapies - The Lancet Neurology
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Deterministic programming of human pluripotent stem cells into microglia facilitates studying their role in health and disease | PNAS
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Cell Type Specific CAG Repeat Expansion and Toxicity of Mutant Huntingtin in Human Striatal and Cerebellar Cell Types | bioRxiv
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Associations between HTT exon one CAG repeat structures and HD clinical... | Download Scientific Diagram
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A library of base editors for the precise ablation of all protein-coding genes in the mouse mitochondrial genome | Nature Biomedical Engineering
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FAN1-MLH1 interaction affects repair of DNA interstrand cross-links and slipped-CAG/CTG repeats | Science Advances
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