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Closer to a cure for Huntington's disease: scientists develop a new CRISPR method that can safely excise CAG repeats from the HTT gene in patient-derived cell lines. If it could be efficiently and safely delivered to Huntington patient brains, it could represent a cure. A big if, obviously.
Closer to a cure for Huntington's disease: scientists develop a new CRISPR method that can safely excise CAG repeats from the HTT gene in patient-derived cell lines. If it could be efficiently and safely delivered to Huntington patient brains, it could represent a cure. A big if, obviously.
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