Researchers pioneer study for rare genetic condition myotonic dystrophy type 1
Researchers in Salford are pioneering a study examining a potential new treatment for people with a rare and currently incurable...
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MoreSalford Royal joins pioneering 100,000 Genomes Project
Salford Royal is helping to change how NHS patients are treated and cared for by taking part in the pioneering...
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More100,000 Genomes Project comes to Salford Royal
Find out about how the 100,000 Genomes Project is changing how NHS patients are treated and cared for at a...