Gene Therapy

New NIH grant helps MU scientist get to the heart of muscular dystrophy

Published in Gene Therapy Weekly, December 23rd, 2010

2010 DEC 23 -- Children with Duchenne muscular dystrophy (DMD) face a future of rapidly weakening muscles, which usually leads to death by respiratory or cardiac failure before their 30th birthday. While researchers are hopeful that gene therapy could eventually evolve into an effective treatment, few have targeted the heart of the problem as much as Dongsheng Duan, PhD.

Duan hopes a new $2.1 million grant he received from the National Institutes of Health will help him develop a treatment that prevents heart muscles from weakening as a result of DMD. As many as 40 percent of patients with the inherited disorder die from heart failure because their weakened...

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Source: Gene Therapy Weekly (2010-12-23)

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