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Progress in therapy for Duchenne muscular dystrophy

✍ Scribed by Rebecca J. Fairclough; Akshay Bareja; Kay E. Davies

Book ID
110110235
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
341 KB
Volume
96
Category
Article
ISSN
0958-0670

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## Abstract This commentary highlights the promising results of recent studies in animal models of Duchenne muscular dystrophy and amyotrophic lateral sclerosis that have clearly demonstrated the potential of gene therapy for tackling these diseases. In the absence of effective drugs or other treat

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## Abstract Mutations in the dystrophin gene cause an X‐linked genetic disorder: Duchenne muscular dystrophy (DMD). Stem cell therapy is an attractive method to treat DMD because a small number of cells are required to obtain a therapeutic effect. Here, we discussed about multiple types of myogenic