Hunting for a cure: the therapeutic potential of gene therapy in Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is an incurable disease and the search for a cure is a challenging journey. However, with recent encouraging progress, we are seeing a light at the end of a long tunnel. This review focuses on several main strategies in gene therapy, including truncated dystrophin g...
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Main Authors: | Hashim, Hasnur Zaman, Che Abdullah, Shahrin Tarmizi, Wan Sulaiman, Wan Aliaa, Hoo, Fan Kee, Basri, Hamidon |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2014
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Online Access: | http://psasir.upm.edu.my/id/eprint/37897/1/Hunting%20for%20a%20cure%20the%20therapeutic%20potential%20of%20gene%20therapy%20in%20Duchenne%20muscular%20dystrophy.pdf http://psasir.upm.edu.my/id/eprint/37897/ http://www.sciencedirect.com/science/article/pii/S101631901400007X |
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