Scientists Turn Muscular Dystrophy Defect On And Off In Cells

For the first time, scientists from the Florida campus of The Scripps Research Institute (TSRI) have identified small molecules that allow for complete control over a genetic defect responsible for the most common adult onset form of muscular dystrophy. These small molecules will enable scientists to investigate potential new therapies and to study the long-term impact of the disease... via Health News from Medical News Today Read More Here..

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