Therapy of Genetic Disorders: Novel Therapies for Duchenne Muscular Dystrophy
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s40124-014-0044-x.pdf
Reference105 articles.
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2. Eagle M, Baudouin SV, Chandler C, et al. Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation. Neuromuscul Disord. 2002;12(10):926–9.
3. England SB, Nicholson LV, Johnson MA, et al. Very mild muscular dystrophy associated with the deletion of 46 % of dystrophin. Nature. 1990;343(6254):180–2.
4. Neri M, Torelli S, Brown S, et al. Dystrophin levels as low as 30 % are sufficient to avoid muscular dystrophy in the human. Neuromuscul Disord. 2007;17(11–12):913–8.
5. Chamberlain JS. Dystrophin levels required for correction of Duchenne muscular dystrophy. Basic Appl Myol. 1997;7:251–5.
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