New gene correction therapy for Duchenne muscular dystrophy

ScienceDaily
Jan 27, 2020, 1:48 pm180 pts
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.

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