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FP42-TH-02 Development of gene therapy for Duchenne muscular dystrophy using systemic delivery of AAV vectors
FP42-TH-02 Development of gene therapy for Duchenne muscular dystrophy using systemic delivery of AAV vectors
2009
Jeffrey S. Chamberlain
Paul Gregorevic
Brian R Schultz
Guy L. Odom
Eric E. Finn
Keywords:
Duchenne muscular dystrophy
Diabetes mellitus
Genetic enhancement
Medicine
Physical therapy
Bioinformatics
Correction
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