[JS-1]Next generation gene therapies for Duchenne muscular dystrophy (DMD)
○Jeffrey Scott Chamberlain, Hichem Tasafout(University of Washington School of Medicine)
Keywords:
Muscle Disease,Gene Therapy,Protein Engineering,Muscle gene expression

Post-doctoral Fellow, Molecular Genetics, Baylor College of Medicine, Houston, Texas, 1985-1990
Assistant, Associate, Full-professor, Dept. of Human Genetics, University of Michigan, Ann Arbor Michigan, USA 1990-2001
Professor and McCaw Chair, Depst. of Neurology, Medicine and Biochemistry, University of Washington, Seattle Washington USA 2001-present
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