Duchenne type muscular dystrophy (DMD) is the most common hereditary muscular disease among children, leaving them wheelchair-bound before the age of twelve and reducing life expectancy. Researchers have developed a gene therapy that may provide permanent relief for those suffering from DMD.
from Top Technology News -- ScienceDaily https://ift.tt/36wSram
Monday, 27 January 2020
New gene correction therapy for Duchenne muscular dystrophy
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