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New RNA therapy to tackle rare childhood diseases | Brimbank & North West
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New RNA therapy to tackle rare childhood diseases | Brimbank & North West
Researchers at St Vincent’s Institute of Medical Research have made a significant breakthrough in developing an novel RNA therapy that could transform the lives of children with rare blood disorders. The cutting-edge RNA Prime Editing technology has the potential to correct the genetic defect that causes life-threatening conditions such as Fanconi anemia, potentially eliminating the need for risky and costly bone marrow transplants. Fanconi anem…
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