Exon skipping for nonsense mutations in Duchenne muscular dystrophy: too many mutations, too few patients?
Author:
Publisher
Informa Healthcare
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology
Link
http://www.tandfonline.com/doi/pdf/10.1517/14712598.2012.693469
Reference104 articles.
1. The Pathology of Paralysis with Muscular Degeneration (Paralysie Myosclerotique), or Paralysis with Apparent Hypertrophy
2. Dystrophin: The protein product of the duchenne muscular dystrophy locus
3. PREDNISONE IN DUCHENNE MUSCULAR DYSTROPHY
4. Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts
5. Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs
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