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Furthermore, cRISPR-Cas9 technology offers transformative potential in treating Huntingtons Disease (HD) by directly addressing its genetic root causes. This manuscript explores the pathophysiological mechanisms of HD, characterized by toxic mutant huntingtin (mHTT) protein resulting from expanded CAG repeats in the HTT gene, and the challenges posed by current therapeutic limitations. We ... This aspect of Learn About Gene Therapy For Huntington S Disease Asgct plays a vital role in practical applications.
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CRISPR-Cas9 technology offers transformative potential in treating Huntingtons Disease (HD) by directly addressing its genetic root causes. This manuscript explores the pathophysiological mechanisms of HD, characterized by toxic mutant huntingtin (mHTT) protein resulting from expanded CAG repeats in the HTT gene, and the challenges posed by current therapeutic limitations. We ... This aspect of Learn About Gene Therapy For Huntington S Disease Asgct plays a vital role in practical applications.
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