Potential New Gene Therapy Strategy For Muscle-Wasting Diseases
Mar 15th 2008Drug InformationMuscular Dystrophy
Investigators in The Research Institute at Nationwide Children’s Hospital have identified the role of a protein that could potentially lead to new clinical treatments to combat musculoskeletal diseases, including Duchenne muscular dystrophy (DMD).Results of these studies appear in the March 11, 2008 issue of the Proceedings of the National Academy of Sciences.
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