Scientists have developed a new approach that could eventually be used to treat Duchenne muscular dystrophy. The stem cell gene therapy could be applicable for 60 percent of people with Duchenne, which affects approximately 1 in 5,000 boys in the US and is the most common fatal childhood genetic disease.
Stem cell gene therapy could be key to treating Duchenne muscular dystrophy
Science Daily - 12 Feb 2016 23:39
Scientists have developed a new approach that could eventually be used to treat Duchenne muscular dystrophy. The stem cell gene therapy could be applicable for 60 percent of people with Duchenne, which affects approximately 1 in 5,000 boys in the US and is the most common fatal childhood genetic disease.
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