Hope emerges for Huntington's patients
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Hope emerges for Huntington's patients
A one-time gene therapy treatment has shown remarkable success in slowing the progression of Huntington's disease in a preliminary trial. The experimental treatment, called AMT-130, reduced disease progression by 75% over three years in patients who received a high dose, compared to those on standard care, according to researchers. While these ...
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Genome editing Gene Therapy
Gene Editing Mechanism of CRISPR-Cas9
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CRISPR Gene Editing Is Being Tested in Human Patients. Here’s What You Need to Know
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