Uploaded November 2025 | Updated September 2026, 2 weeks ago

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Check out our explainer here: youtube.com/watch?v=g66x9funPc0

Scientists have developed a one-time gene therapy, AMT-130, that significantly slows the progression of Huntington's disease by targeting and silencing the mutant huntingtin protein in the brain. In a Phase I/II trial, this therapy reduced disease progression by 75% over one year, preserving motor and cognitive functions.

#medicine #breakthrough #huntingtonsdisease #neuroscience #shorts

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