Friday, September 11, 2020

Drugging the undruggable: Treatment path for muscular dystrophy

Researchers have identified a possible treatment for Duchenne muscular dystrophy (DMD), a rare genetic disease for which there is currently no cure or treatment, by targeting an enzyme that had been considered 'undruggable.'

from Health & Medicine News -- ScienceDaily https://www.sciencedaily.com/releases/2020/09/200911141747.htm

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